WO2019204819A1 - Aminopyrazines and related compounds useful as mitochondrial uncouplers - Google Patents

Abstract

The disclosure provides compounds of Formula I and the pharmaceutically acceptable salts thereof. The variables, R¹, R², R³, R⁴, R⁵, X¹, X², and Z are defined herein. Certain compounds of Formula I act as selective mitochondrial protonophore uncouplers that do not affect the plasma membrane potential. The disclosure includes pharmaceutical composition comprising a compound or salt Formula I, and a pharmaceutically acceptable carrier. Compounds and salts of Formula I are useful for treating or decreasing the risk of conditions responsive to mitochondrial uncoupling, such as obesity, cancer, type II diabetes, fatty liver disease, insulin resistance, Parkinson's disease, ischemia reperfusion injury, heart failure, non-alcoholic fatty liver disease (NALFD), and non-alcoholic steatohepatitis (NASH). Because mitochondrial uncouplers decrease the production of reactive oxygen species (ROS), which are known to contribute to age-related cell damage, compounds of Formula I are useful for increasing lifespan. Compounds and salts of Formula I are also useful for regulating glucose homeostasis or insulin action in a patient.

Description

AMIN OPYR AZINES AND RELATED COMPOUNDS USEFUL AS MITOCHONDRIAL

UNCOUPLERS

CROSS REFERENCE TO RELATED APPLICATION

[0001] This application claims priority of U.S. Provisional Appl. No. 62/660,880, filed April 20, 2018, which is hereby incorporated by reference in its entirety.

BACKGROUND

[0002] Cellular respiration is a physiological process with a fundamental goal of producing energy in the form of ATP. During cellular respiration, chemical energy derived from nutrients is converted into ATP. Specifically, the oxidation of nutrients in the mitochondrial matrix generates high- energy electron carriers nicotinamide adenine dinucleotide (NADH) and flavin adenine dinucleotide (FADH2) that are oxidized by the mitochondrial electron transport chain (ETC) located in the

mitochondrial inner-membrane (MIM). Electron flow through the ETC is an exergonic process that drives a series of proton pumps to efflux protons from the matrix into the inter-membrane space (IMS) against their concentration gradient. The resulting proton concentration (ApH) and electrical (DY) gradient is known as the proton-motive force (pmf). Protons that re-enter the mitochondrial matrix via ATP synthase drive endergonic production of ATP. Thus, mitochondrial ATP production involves the coupling of electron transport to phosphorylation reactions via a proton gradient across the MIM.

[0003] Mitochondrial uncoupling describes processes that uncouple nutrient oxidation from ATP production. Mitochondrial uncoupling is a normal physiological process that occurs as either basal or inducible proton leak from the intermembrane space. Basal proton leak accounts for -20-25% of the basal metabolic rate of mammals. The reason for such metabolic inefficiency is not entirely understood; however, membrane lipid composition and abundance of the adenine nucleotide translocase (ANT) are factors that contribute to basal rates of proton leak. Induced proton leak is driven by reactive species and fatty acids that activate uncoupling proteins (UCPs). UCPs are located in the MIM and facilitate the transfer protons into the matrix independent of ATP synthase.

[0004] There are five known UCPs in mammals, UCP1-5, that have distinct tissue localization. The best-characterized UCPs are UCP1 and UCP2. UCP1 is expressed in brown and beige adipose tissue and has a role in non-shivering thermogenesis. UCP1 is unlikely to operate as a simple proton channel, but instead transfers protons via a mechanism that requires long-chain fatty acids. In contrast, UCP2 has a broad tissue distribution and no role in thermogenesis. UCP2 uncouples mitochondria to prevent hyperpolarization and decrease mitochondrial superoxide production. [0005] Small molecule mitochondrial uncouplers either act directly as protonophores by transporting protons into the matrix independently of protein complexes or, alternatively, mediate uncoupling via proteins such as ANT. Protonophoric uncouplers are lipophilic enough to enable passage through the MIM and weakly acidic to enable partial and reversible pH-dependent ionization.

Mitochondrial uncoupling has two major phenotypes of therapeutic relevance including increased nutrient oxidation to compensate for lack of efficiency in ATP production and decreasing superoxide production from the ETC. The ETC is a primary source of reactive oxygen species (ROS) in most tissues. ETC- derived superoxide formation occurs via a non-enzymatic process when single electrons on co-enzymes or prosthetic groups in redox centers interact with molecular oxygen. Single electrons in the ETC only transiently exist in redox centers and the dwell time for single electrons in an unstable state increases the likelihood of superoxide production. Mitochondrial uncouplers decrease mitochondrial superoxide production by stimulating faster electron transfer that decreases the dwell time for single electrons in the ETC.

[0006] The therapeutic potential of mitochondrial uncouplers is related to their dual roles in increasing nutrient oxidation and decreasing ROS production from the ETC. On the one hand, increased nutrient oxidation promotes leanness and is a therapeutic strategy to treat obesity and related metabolic diseases. On the other hand, mitochondrial ROS are linked to numerous pathologies including ischemia- reperfusion injury, inflammation, insulin resistance, neurodegeneration, and many other pathologies. Importantly, mitochondrial uncouplers prevent ROS production, which is advantageous compared to antioxidants that scavenge ROS that has already been produced. As such, decreasing mitochondrial ROS production has significant therapeutic potential with advantages over antioxidant scavengers.

[0007] Mitochondria regulate cellular metabolism and play an important role in the pathogenesis of some of the most prevalent human diseases including obesity, cancer, diabetes, neurodegeneration, and heart disease. Many of these diseases can be improved by the use of pharmacological agents like mitochondrial uncouplers that lessen mitochondrial oxidative damage and increase energy expenditure. Genetic and pharmacologic uncoupling have beneficial effects on disorders that are linked to

mitochondrial oxidative stress, such as ischemic-reperfusion injury, Parkinson’s disease, insulin resistance, aging, and heart failure, and disorders that stand to benefit from increased energy expenditure such as obesity.

[0008] Mitochondrial uncouplers are known and have been shown to be effective for treating obesity. For example, 2,4-dinitrophenol (DNP) is a well-known small molecule mitochondrial protonophore that results in weight loss in humans. Patients consuming -300 mg/d steadily shed an average of 1.5 pounds per week over the course of several months without changes in food intake.

Similarly, mice treated with DNP demonstrate improved serological glucose, triglyceride, and insulin levels, as well as decreased oxidative damage, reduced body weight, and increased longevity. Flowever, DNP has off-target effects on other cellular membranes resulting in a narrow therapeutic index. DNP was subsequently withdrawn from the North American market by the US Food and Drug Administration in 1938. Currently, there are no uncoupler drugs that are safe enough for use in humans.

[0009] The development of a selective mitochondrial protonophore uncoupler that does not affect the plasma membrane potential would broaden the safety margin of mitochondrial uncouplers and provide renewed hope that mitochondrial uncoupling can be targeted for the treatment of obesity, type II diabetes, and other diseases, disorders, and conditions related to mitochondrial function. There is a long felt need in the art for compositions and methods useful for preventing and treating obesity, diabetes, regulating glucose homeostasis, reducing adiposity, protecting from ischemic-reperfusion injury, and regulating insulin action using mitochondrial uncouplers as well as for compounds useful as

mitochondrial uncouplers. The present disclosure satisfies these needs.

SUMMARY

[0010] This disclosure provides compounds of Formula I,

(Formula I)

and the pharmaceutically acceptable salt thereof. The variables in Formula I, e.g. X¹, X², Z, and R¹ - R⁵ carry the following values.

[0011] X¹ and X² are chosen from N and CH, wherein at least one of X¹ and X² is N.

[0012] Z is absent (R² is bound to N) or Z is -C(=0)-.

[0013] R¹ is hydrogen or Ci-Csalkyl, C2-Csalkenyl, or C2-Csalkynyl.

[0014] R² is Ci-Csalkyl, C2-Csalkenyl, or C2-Csalkynyl; or

R² is -Co-C4alkyl(C3-C7cycloalkyl), -Co-C4alkyl(bridged C7-Ci2cycloalkyl),

-Co-C4alkyl(aryl), -Co-C4alkyl(mono- or bi-cyclic heteroaryl), or -Co-C₄alkyl(3- to 7- membered heterocycloalkyl), each of which is optionally substituted with one or more substituents independently chosen from R¹¹ and 0 or 1 substituents R¹².

[0015] R³ is H or Ci-Csalkyl, C2-Csalkenyl, or C2-Csalkynyl, or

R³ is -Co-C4alkyl(C3-C7cycloalkyl) or -Co-C4alkyl(aryl), which is optionally substituted with one or more independently chosen R¹¹ substituents.

R⁴ and R⁵ are independently selected from halogen, hydroxyl, amino, nitro, cyano, -CHO, - COOH, Ci-C2haloalkyl, Ci-C2haloalkoxy, CVO.alkyl, CVO.alkoxy, Ci-O.alkylcstcr, -Co-C4alkyl(mono- or di -C i -0,al kyl am i no) , C2-C6alkanoyl, C2-C6alkenyl, C2-C6alkynyl, Wherein in each Co-C4alkyl, Ci- Csalkyl, Ci-C^alkyl, C2-Csalkenyl, or C2-Csalkynyl, aryl, optionally substituted with R¹³, and mono- or bicyclic heteroaryl, optionally substituted with R¹³.

[0016] In the definitions of R¹, R², and R³ one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-, -C(0)0-, -OC(O), -S(0)n-, -C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the Co-C4alkyl, Ci-Cs alkyl, C2-Csalkenyl, or C2-Csalkynyl is optionally substituted with one or more substituents R¹³.

[0017] R¹⁰ is independently chosen at each occurrence from hydrogen, CVO, alkyl, and -Co- C₂alkyl(C₃ -C7cycloalkyl) .

[0018] R¹¹ is independently selected at each occurrence from halogen, hydroxyl, amino, nitro, cyano, -CHO, -COOH, oxo, halosulfanyl, and Ci-Cioalkyl, C2-Csalkenyl, and C2-Csalkynyl, wherein in each Ci-Cioalkyl, C2-Csalkenyl, and C2-Csalkynyl, in the definition of R¹¹ one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-, -C(0)0-, -OC(O), -S(0)n-, -S(0)nNR¹⁰, -NR¹⁰S(O)n-, - NR¹⁰C(O)NR¹⁰,

-C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which each Co-C4alkyl, Ci-Csalkyl, C2-Csalkenyl, or C2-Csalkynyl is optionally substituted with one or more substituents R¹³.

[0019] R¹² is selected from -Co-C4alkyl(C3-C7cycloalkyl), -0-Co-C₄alkyl(C₃-C₇cycloalkyl), -Co- C4alkyl(aryl), -0-Co-C₄alkyl(aryl), -Co-C₄alkyl(5- to 6-membered heteroaryl), -0-Co-C₄alkyl(5- to 6- membered heteroaryl), -Co-C₄alkyl(3- to 6-membered heterocycloalkyl), and -0-Co-C₄alkyl(3- to 6- membered heterocycloalkyl), each of which is optionally substituted with one or more substituents independently chosen from halogen, hydroxyl, amino, nitro, cyano, -CHO, -COOH, oxo, Ci-C2haloalkyl, Ci-C2haloalkoxy, CVO, alkyl, CVO.alkoxy, Ci-C_r, alkyl ester, -Co-C4alkyl(mono- or di -CV , alkyl ami no), C2-C6alkanoyl, C2-C6alkenyl, and C2-C6alkynyl.

[0020] R¹³ is independently chosen at each occurrence from halogen, hydroxyl, amino, nitro, cyano, -CHO, -COOH, oxo, Cs-Ocycloalkyl, and phenyl.

[0021] The disclosure includes a pharmaceutical composition, comprising a compound or salt of Formula I, together with a pharmaceutically acceptable excipient.

[0022] The disclosure includes a method of treating or preventing a condition responsive to mitochondrial uncoupling, comprising administering a therapeutically effective amount of a compound or salt of Formula I to a patient in need of such treatment. Conditions responsive to mitochondrial uncoupling include obesity, type II diabetes, fatty liver disease, insulin resistance, Parkinson’s disease, ischemia reperfusion injury, heart failure, non-alcoholic fatty liver disease (NALFD), and non-alcoholic steatohepatitis (NASH). [0023] The disclosure includes a method of regulating glucose homeostasis or insulin action in a patient comprising administering a therapeutically effective amount of a compound or salt of Formula I to a patient in need thereof.

[0024] The disclosure also includes a method of treating hyperlipidemia, glycemia, glucose tolerance, insulin sensitivity, adiposity, insulin resistance, obesity, or diabetes in a patient comprising administering a therapeutically effective amount of a compound of Formula I to the patient.

[0025] In the description and claims, terms will carry the definitions set forth in this section unless the stated otherwise or contrary to the context. Unless defined otherwise, all technical and scientific terms used herein have the commonly understood by one of ordinary skill in the art to which the disclosure pertains. Although any methods and materials similar or equivalent to those described herein may be useful in the practice or testing of the embodiments of this disclosure; preferred methods and materials are described below.

[0026] The terms“a” and“an” do not denote a limitation of quantity, but rather denote the presence of at least one of the referenced item. The term“or” means“and/or”. The term "about,” as used herein, means approximately, in the region of, roughly, or around. When the term "about" is used in conjunction with a numerical range, it modifies that range by extending the boundaries above and below the numerical values set forth. In general, the term“about” is used herein to modify a numerical value above and below the stated value by a variance of 10%. Therefore, about 50% means in the range of 45%- 55%.

[0027] Numerical ranges recited herein by endpoints include all numbers and fractions subsumed within that range (e.g. 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.90, 4, and 5).

[0028] The terms“additional therapeutically active compound” or“additional therapeutic agent,” refers to the use or administration of a compound for an additional therapeutic use for a particular injury, disease, or disorder being treated. Such a compound, for example, could include one being used to treat an unrelated disease or disorder, or a disease or disorder which may not be responsive to the primary treatment for the injury, disease or disorder being treated.

[0029] As used herein, the terms“administration of’ and or“administering” a compound should be understood to mean providing a compound of the disclosure to a subject in need of treatment.

[0030] An“agonist” is a composition of matter which, when administered to a mammal such as a human, enhances or extends a biological activity attributable to the level or presence of a target compound or molecule of interest in the subject.

[0031] “Alleviating a disease or disorder symptom,” means reducing the severity of the symptom or the frequency with which such a symptom is experienced by a subject, or both. [0032] An“antagonist” is a composition of matter which when administered to a mammal such as a human, inhibits a biological activity attributable to the level or presence of a compound or molecule of interest in the subject.

[0033] A“Compound of Formula I” as used herein, refers to any compound within the scope of Formula I and, unless the context indicates otherwise, includes the pharmaceutically acceptable salts of Formula I.

[0034] The terms“comprises,”“comprising,” and the alternate transitional phrases“includes,” “including,”“contain,” and“containing” are open ended transitional phrases having the meaning ascribed to them in U.S. Patent Law. “Comprises” and the other open-ended terms encompass the intermediate term“consisting essentially of’ and the closed ended terms“consisting of’ and“consists of.” Claims reciting one of the open-ended transitional phrases can be written with any other transitional phrase, which may be more limiting, unless clearly precluded by the context or art.

[0035] The term“delivery vehicle” refers to any kind of device or material which can be used to deliver compounds in vivo or can be added to a composition comprising compounds administered to a plant or animal. This includes, but is not limited to, implantable devices, aggregates of cells, matrix materials, gels, etc.

[0036] A“disease” is a state of health of an animal wherein the animal cannot maintain homeostasis, and wherein if the disease is not ameliorated then the animal’s health continues to deteriorate. In contrast, a“disorder” in an animal is a state of health in which the animal is able to maintain homeostasis, but in which the animal’s state of health is less favorable than it would be in the absence of the disorder. Left untreated, a disorder does not necessarily cause a further decrease in the animal’s state of health.

[0037] As used herein, an“effective amount” or“therapeutically effective amount” means an amount sufficient to produce a selected effect, such as alleviating symptoms of a disease or disorder. In the context of administering compounds in the form of a combination, such as multiple compounds, the amount of each compound, when administered in combination with another compound(s), may be different from when that compound is administered alone. Thus, an effective amount of a combination of compounds refers collectively to the combination as a whole, although the actual amounts of each compound may vary.

[0038] As used in the specification and the appended claims, the terms“for example,”“for instance,”“such as,”“including” and the like are meant to introduce examples that further clarify more general subject matter. Unless otherwise specified, these examples are provided only as an aid for understanding the disclosure and are not meant to be limiting in any fashion.

[0039] The terms“formula” and“structure” are used interchangeably herein. [0040] The term“inhibit,” as used herein, refers to the ability of a compound of the disclosure to reduce or impede a described function, such as having inhibitory sodium channel activity. Preferably, inhibition is by at least 10%, more preferably by at least 25%, even more preferably by at least 50%, and most preferably, the function is inhibited by at least 75%. The terms“inhibit”,“reduce”, and“block” are used interchangeably herein.

[0041] As used herein“injecting or applying” includes administration of a compound of the disclosure by any number of routes and means including, but not limited to, topical, oral, buccal, intravenous, intramuscular, intra-arterial, intramedullary, intrathecal, intraventricular, transdermal, subcutaneous, intraperitoneal, intranasal, enteral, topical, sublingual, vaginal, ophthalmic, pulmonary, or rectal means.

[0042] As used herein, an“instructional material” includes a publication, a recording, a diagram, or any other medium of expression which can be used to communicate the usefulness of compound of the disclosure in the kit for effecting alleviation of the various diseases or disorders recited herein.

Optionally, or alternately, the instructional material may describe one or more methods of alleviating the diseases or disorders in a cell or a tissue of a mammal. The instructional material of the kit of the disclosure may, for example, be affixed to a container which contains the identified disclosure compound or be shipped together with a container which contains the identified compound.

[0043] Alternatively, the instructional material may be shipped separately from the container with the intention that the instructional material and the compound be used cooperatively by the recipient.

[0044] The term,“mitochondrial uncoupling,” also referred to as“uncoupling,” refers to the process whereby protons enter the mitochondrial matrix via a pathway independent of ATP synthase and thereby uncouple nutrient oxidation from ATP production. This process can be pharmacologically induced by small molecule mitochondrial protonophores, which directly shuttle protons across the mitochondrial inner membrane into the matrix. The primary pathway for energy production in aerobic cells involves the oxidation of nutrients (including fats, carbohydrates, and amino acids) in mitochondria, which promotes the efflux of protons out of the mitochondrial matrix. This process creates a pH and electrochemical gradient across the mitochondrial inner membrane. Protons normally re-enter the mitochondrial matrix via ATP synthase, which results in ATP production. Protons can also re-enter the mitochondrial matrix via pathways independent of ATP synthase, which‘uncouples’ nutrient oxidation and proton efflux from ATP production.

[0045] The term“modulate,” means changing the level of an activity, function, or process. The term“modulate” encompasses both inhibiting and stimulating an activity, function, or process.

[0046] As used herein,“parenteral administration” of a pharmaceutical composition includes any route of administration characterized by physical breaching of a tissue of a subject and administration of the pharmaceutical composition through the breach in the tissue. Parenteral administration thus includes, but is not limited to, administration of a pharmaceutical composition by injection of the composition, by application of the composition through a surgical incision, by application of the composition through a tissue-penetrating non-surgical wound, and the like. In particular, parenteral administration is contemplated to include, but is not limited to, subcutaneous, intraperitoneal, intramuscular, intrasternal injection, and kidney dialytic infusion techniques.

[0047] The term“per application” as used herein refers to administration of a compositions, drug, or compound to a subject.

[0048] The term“pharmaceutical composition” shall mean a composition comprising at least one active ingredient and a pharmaceutically acceptable carrier, such as a pharmaceutically acceptable excipient.

[0049] A“pharmaceutically acceptable excipient” means an excipient that is useful in preparing a pharmaceutical composition/ combination that is generally safe, non-toxic and neither biologically nor otherwise undesirable, and includes an excipient that is acceptable for veterinary use as well as human pharmaceutical use. The term also encompasses any of the inactive agents approved for use

pharmaceutical compositions in by a regulatory agency of the US Federal government or listed in the US Pharmacopeia for use in animals, including humans.

[0050] The term“pharmaceutically acceptable carrier” includes any of the standard pharmaceutical carriers, such as a phosphate buffered saline solution, water, emulsions such as an oil/water or water/oil emulsion, and various types of wetting agents. The term also encompasses any of the agents approved by a regulatory agency of the US Federal government or listed in the US

Pharmacopeia for use in animals, including humans.

[0051] “Pharmaceutically acceptable” means physiologically tolerable, for either human or veterinary application. As used herein,“pharmaceutical compositions” include formulations for human and veterinary use.

[0052] “Plurality” means at least two.

[0053] The term“prevent,” as used herein, means to stop something from happening or to significantly reduce the likelihood of something happening, such as by taking advance measures against something possible or probable outcome. In the context of medicine,“prevention” includes an action taken to decrease the chance of getting a disease or condition.

[0054] A "preventive" or "prophylactic" treatment is a treatment administered to a subject who does not exhibit signs, or exhibits only early signs, of a disease or disorder. A prophylactic or preventative treatment is administered for the purpose of decreasing the risk of developing pathology associated with developing the disease or disorder. [0055] A“prodrug” refers to an agent that is converted into the parent drug in vivo. Prodrugs are often useful because, in some situations, they may be easier to administer than the parent drug. They may, for instance, be bioavailable by oral administration whereas the parent is not. The prodrug may also have improved solubility in pharmaceutical compositions over the parent drug, or may demonstrate increased palatability or be easier to formulate.

[0056] A“subject” of analysis, diagnosis, or treatment is an animal. Such animals include mammals, preferably a human. As used herein, a“subject in need thereof’ is a patient, animal, mammal, or human, who will benefit from the method of this disclosure.

[0057] The term“symptom,” as used herein, refers to any morbid phenomenon or departure from the normal in structure, function, or sensation, experienced by the patient and indicative of disease. In contrast, a“sign” is objective evidence of disease. For example, a bloody nose is a sign. It is evident to the patient, doctor, nurse and other observers.

[0058] A“therapeutic” treatment is a treatment administered to a subject who exhibits signs of pathology for the purpose of diminishing or eliminating those signs.

[0059] A“therapeutically effective amount” of a compound is that amount of compound which is sufficient to provide a beneficial effect to the subject to which the compound is administered.

[0060] As used herein,“treat,”“treating”, or“treatment” includes treating, ameliorating, or inhibiting an injury or disease related condition or a symptom of an injury or disease related condition. In one embodiment the disease, injury or disease related condition or a symptom of an injury or disease related condition is prevented; while another embodiment provides prophylactic treatment of the injury or disease related condition or a symptom of an injury or disease related condition.

CHEMICAL DEFINITIONS

[0061] “Alkyl” is a branched or straight chain saturated aliphatic hydrocarbon group, having the specified number of carbon atoms, generally from 1 to about 8 carbon atoms. The term CVCValkyl as used herein indicates an alkyl group having from 1, 2, 3, 4, 5, or 6 carbon atoms. Other embodiments include alkyl groups having from 1 to 6 carbon atoms, 1 to 4 carbon atoms or 1 or 2 carbon atoms, e.g. Ci-Cs-alkyl, Ci-C4-alkyl, and Ci-C2-alkyl. Examples of alkyl include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, 3-methylbutyl, t-butyl, n-pentyl, sec-pentyl, heptyl, and octyl. “Co-C_n alkyl” is used together with another group, e.g. Co-C4alkyl(C3-C7cycloalkyl), to indicate the other group, in this case C3-C7cycloalkyl, is bound to the group it substitutes either by a single covalent bond (Co) or attached through an alkylene linker having the indicated number of carbon atoms.

[0062] “Alkenyl” is a branched or straight chain aliphatic hydrocarbon group having one or more double carbon-carbon bonds that may occur at any stable point along the chain, having the specified number of carbon atoms. Examples of alkenyl include, but are not limited to, ethenyl, propenyl, 1, 3- butadienyl, l-butenyl, hexenyl, and pentenyl.

[0063] “Alkynyl” is a branched or straight chain aliphatic hydrocarbon group having one or more triple carbon-carbon bonds that may occur at any stable point along the chain, having the specified number of carbon atoms. Examples of alkynyl include, but are not limited to, ethynyl, propynyl, 1- butynyl, 2-butynyl, and l-pentynyl.

[0064] “Alkanoyl” is an alkyl group as defined above covalently bound to the group it substitutes by an carbonyl bridge (-C(=0)-). The carbonoyl oxygen is included in the count of carbons in the substituted group. A C2alkanoyl is -C(=0)CH₃.

[0065] “Alkoxy” is an alkyl group as defined above with the indicated number of carbon atoms covalently bound to the group it substitutes by an oxygen bridge (-0-). Examples of alkoxy include, but are not limited to, methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, 2-butoxy, t-butoxy, n-pentoxy, 2-pentoxy, 3- pentoxy, isopentoxy, neopentoxy, n-hexoxy, 2-hexoxy, 3-hexoxy, and 3- methylpentoxy.

[0066] “Alkylamino” is an alkyl group as defined herein covalently bound to the group it substitutes by an amino linkage. An alkylamino group can be a mono-alkyl group in which the amino is a secondary amino (alkylNH-) or a di-alkyl group in which the amino is a tertiary amino (alkyll)(alkyl2)N- . The alkyl groups of a di-alkylamino are the same or different.

[0067] “Alkylester” is an alkyl group as defined herein covalently bound to the group it substitutes by an ester linkage. The ester linkage may be in either orientation, e.g., a group of the formula -OC(0)-alkyl or a group of the formula -C(0)0-alkyl.

[0068] "Aryl" indicates a mono-, bi- or tri-cyclic ring system having at least one aromatic ring. Aryl groups contain only carbon in the aromatic ring or rings. An aryl group may be fused to a non aromatic ring containing N, O, or S heteroatoms. Typical aryl groups contain 1 to 3 separate, fused, or pendant rings and from 6 to about 18 ring atoms, without heteroatoms as ring members. When indicated, such aryl groups may be further substituted with carbon or non-carbon atoms or groups. Example include phenyl, naphthyl, bi-phenyl, tetrahydronaphthyl, indanyl, and indenyl group.

[0069] “Cycloalkyl” is a saturated hydrocarbon ring group, having the specified number of carbon atoms. Monocyclic cycloalkyl groups typically have from 3 to about 8 carbon ring atoms, from 3 to 7 ring atoms, or from 3 to 6 (3, 4, 5, or 6) carbon ring atoms. Cycloalkyl substituents may be pendant from a substituted nitrogen, oxygen, or carbon atom, or a substituted carbon atom that may have two substituents may have a cycloalkyl group, which is attached as a spiro group. Examples of cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.

[0070] A“bridged cycloalkyl” is a cycloalkyl group that has two or more rings containing only carbon ring atoms, and one of the carbon rings contains a“bridge” of 1 carbon atom or 2-3 unbranched carbon atoms connected to two“bridgehead” atoms in the carbon ring. The bridgehead atoms are usually non-adjacent carbon ring atoms. Examples of bridge cycloalkyl groups include, but are not limited to, bicyclo[2.2.2]octanyl, bicyclo[3.3.l]nonanyl, adamantanyl, and and bicyclo[3.3.3]undecanyl groups.

“Halogen” or“halo” includes bromo, chloro, fluoro, and iodo.

[0071] “Haloalkyl” indicates both branched and straight-chain alkyl groups having the specified number of carbon atoms, substituted with 1 or more halogen atoms, up to the maximum allowable number of halogen atoms. Examples of haloalkyl include, but are not limited to, trifluoromethyl, difluoromethyl, 2-fluoroethyl, 2,2,2-trifluoroethyl, and penta-fluoroethyl.

[0072] “Haloalkoxy” indicates a haloalkyl group as defined herein attached through an oxygen bridge (oxygen of an alcohol radical).

[0073] “Halosulfanyl” is a sulfur substituted with one or more halogen atoms, up to the maximum allowable number of halogen atoms.

[0074] “Heteroaryl” is a ring or ring system having at least one aromatic ring containing a heteroatom independently chosen from N, O, and S with remaining ring atoms being carbon. Fused rings may or may not contain heteroatoms and need not be aromatic. It is preferred that the total number of heteroatoms in a heteroaryl ring system is not more than 4 and that the total number of S and O atoms in a heteroaryl ring system is not more than 2. Monocyclic heteroaryl groups typically have from 5 to 7 ring atoms. In some embodiments bicyclic heteroaryl groups are 9- to lO-membered heteroaryl groups, that is, groups containing 9 or 10 ring atoms in which one 5- to 7-member aromatic ring is fused to a second aromatic or non-aromatic ring. When the total number of S and O atoms in an aromatic ring of the heteroaryl group exceeds 1, these heteroatoms are not adjacent to one another. Examples of heteroaryl groups include, but are not limited to, oxazolyl, pyranyl, pyrazinyl, pyrazolopyrimidinyl, pyrazolyl, pyridazinyl, pyridyl, pyrimidinyl, pyrrolyl, quinolinyl, tetrazolyl, thiazolyl, thienylpyrazolyl, thiophenyl, triazolyl, benzol c/]oxazolyl, benzofuranyl, benzothiazolyl, benzothiophenyl, benzoxadiazolyl, dihydrobenzodioxynyl, furanyl, imidazolyl, indolyl, and isoxazolyl.

[0075] “Heterocycloalkyl” is a saturated cyclic group containing 1 or more ring atoms independently chosen from N, O, and S with remaining ring atoms being carbon. Examples of heterocycloalkyls include tetrahydropyranyl, tetrahydrofuranyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, oxazolidinyl, tetrahydrothiophenyl, tetrahydrothiopyranyl, thiazolidinyl, and pyrrolidinyl.

[0076] “Pharmaceutically acceptable salts” includes derivatives of the disclosed compounds in which the parent compound is modified by making inorganic and organic, non-toxic, acid or base addition salts thereof. The salts of the present compounds can be synthesized from a parent compound that contains a basic or acidic moiety by conventional chemical methods. Generally, such salts can be prepared by reacting free acid forms of these compounds with a stoichiometric amount of the appropriate base (such as Na, Ca, Mg, or K hydroxide, carbonate, bicarbonate, or the like), or by reacting free base forms of these compounds with a stoichiometric amount of the appropriate acid. Alkali metal (for example, sodium, potassium or lithium) or alkaline earth metal (for example calcium) salts of organic (e.g., carboxylic) acids can also be made.

[0077] Such reactions are typically carried out in water or in an organic solvent, or in a mixture of the two.

[0078] Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines or nitrogen-containing heteroaryl rings (e.g. pyridine, quinoline, isoquinoline); alkali or organic salts of acidic residues such as carboxylic acids; and the like. The pharmaceutically acceptable salts include the conventional non-toxic salts and the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids. For example, conventional non-toxic acid salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, phosphoric, nitric and the like; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, malonic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, mesylic, esylic, besylic, sulfanilic, 2-ace toxybenzoic, fumaric, succinic, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, a-ketoglutarate, a-glycerophosphate, isethionic, HCEC CtE CCEH where n is 0-4, and the like.

[0079] Salts derived from inorganic bases, include by way of example only, sodium, potassium, lithium, ammonium, calcium and magnesium salts. Salts derived from organic bases include, but are not limited to, salts of primary, secondary and tertiary amines, such as alkyl amines, dialkyl amines, trialkyl amines, substituted alkyl amines, di(substituted alkyl) amines, tri(substituted alkyl) amines, alkenyl amines, dialkenyl amines, trialkenyl amines, substituted alkenyl amines, di(substituted alkenyl) amines, tri(substituted alkenyl) amines, cycloalkyl amines, di(cycloalkyl) amines, tri(cycloalkyl) amines, substituted cycloalkyl amines, disubstituted cycloalkyl amine, trisubstituted cycloalkyl amines, cycloalkenyl amines, di(cycloalkenyl) amines, tri(cycloalkenyl) amines, substituted cycloalkenyl amines, disubstituted cycloalkenyl amine, trisubstituted cycloalkenyl amines, aryl amines, diaryl amines, triaryl amines, heteroaryl amines, diheteroaryl amines, triheteroaryl amines, heterocyclic amines, diheterocyclic amines, triheterocyclic amines, mixed di- and tri-amines where at least two of the substituents on the amine are different and are selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, cycloalkyl, substituted cycloalkyl, cycloalkenyl, substituted cycloalkenyl, aryl, heteroaryl, heterocyclic, and the like. Also included are amines where the two or three substituents, together with the amino nitrogen, form a heterocyclic or heteroaryl group. Examples of suitable amines include, by way of example only, isopropylamine, trimethyl amine, diethyl amine, tri(iso-propyl) amine, tri(n-propyl) amine, ethanolamine, 2-dimethylaminoethanol, tromethamine, lysine, arginine, histidine, caffeine, procaine, hydrabamine, choline, betaine, ethylenediamine, glucosamine, Nalkylglucamines, theobromine, purines, piperazine, piperidine, morpholine, Nethylpiperidine, and the like. It should also be understood that other carboxylic acid derivatives would be useful in the practice of this disclosure, for example, carboxylic acid amides, including carboxamides, lower alkyl carboxamides, dialkyl carboxamides, and the like.

[0080] Lists of additional suitable salts may be found, e.g., in G. Steffen Paulekuhn, et al, Journal of Medicinal Chemistry 2007, 50, 6665 and Handbook of Pharmaceutical Salts: Properties, Selection and Use, P. Heinrich Stahl and Camille G. Wermuth, Editors, Wiley-VCH, 2002.

[0081] The term“substituted” means that any one or more hydrogens on the designated atom or group is replaced with a selection from the indicated group, provided that the designated atom's normal valence is not exceeded. Unless otherwise specified, each substituent is selected independently of other substituents.“Optionally substituted” means that 0 to the maximum allowable number of substituents are present. When the substituent is oxo (i.e., =0) then 2 hydrogens on the atom are replaced. When an oxo group substitutes a heteroaromatic moiety, the resulting molecule can sometimes adopt tautomeric forms. For example a pyridyl group substituted by oxo at the 2- or 4-position can sometimes be written as a pyridine or hydroxypyridine. Combinations of substituents and/or variables are permissible only if such combinations result in stable compounds or useful synthetic intermediates. A stable compound or stable structure is meant to imply a compound that is sufficiently robust to survive isolation from a reaction mixture and subsequent formulation into an effective therapeutic agent. Unless otherwise specified, substituents are named into the core structure. For example, it is to be understood that aminoalkyl means the point of attachment of this substituent to the core structure is in the alkyl portion and alkylamino means the point of attachment is a bond to the nitrogen of the amino group. However, a dash

indicates a point of attachment for a substituent. -Ci C4alkyl(cycloalkyl) is attached at the 1 to 4 carbon alkylene linker.

[0082] Certain compounds of the disclosure may contain one or more asymmetric elements such as stereogenic centers, stereogenic axes and the like, e.g. asymmetric carbon atoms, so that the compounds can exist in different stereoisomeric forms. These compounds can be, for example, racemates or optically active forms. For compounds with two or more asymmetric elements, these compounds can additionally be mixtures of diastereomers. For compounds having asymmetric centers, it should be understood that all of the optical isomers and mixtures thereof are encompassed. In these situations, single enantiomers, i.e., optically active forms, can be obtained by asymmetric synthesis, synthesis from optically pure precursors, or by resolution of the racemates. Resolution of the racemates can also be accomplished, for example, by conventional methods such as crystallization in the presence of a resolving agent, or chromatography, using, for example using a chiral HPLC column. In addition, compounds with carbon-carbon double bonds may occur in Z- and E-forms, with all isomeric forms of the compounds being included in the present disclosure.

[0083] The disclosure includes deuterated compounds of Formula A and Formula I in which any hydrogen is replaced by a deuterium.“Deuterated” mean that a hydrogen at the specified position is replaced by deuterium. In any sample of a compound of Formula I in which a position is deuterated some discrete molecules of the compound of Formula I will likely have hydrogen, rather than deuterium, at the specified position. However the percent of molecules of the compound of Formula I in the sample which have deuterium at the specified position will be much greater than would naturally occur. The deuterium at the deuterated position is enriched. The term“enriched” as used herein, refers to the percentage of deuterium versus other hydrogen species at that location. As an example, if it is said that a position in the compound of Formula I contains 50% deuterium enrichment, that means that rather than hydrogen at the specified position the deuterium content is 50%. For clarity, it is confirmed that the term“enriched” as used herein does not mean percentage enriched over natural abundance. In one embodiment, deuterated compounds of Formula I will have at least 10% deuterium enrichment at any deuterated position. In other embodiments, there will be at least 50%, at least 90%, or at least 95% deuterium enrichment at the specified deuterated position or positions. A“deuterated substituent” is a substituent in which at least one hydrogen is replaced by deuterium at the specified percent enrichment.- Optionally deuterated” means that the position may be at either hydrogen and the amount of deuterium at the position is only the naturally occurring level of deuterium or the position is enriched with deuterium above the naturally occurring deuterium level.

[0084] Where a compound exists in various tautomeric forms, the disclosure is not limited to any one of the specific tautomers, but rather includes all tautomeric forms. The compounds of the disclosure may exist in tautomeric forms both mixtures and separate individual tautomers are included. For example

CHEMICAL DESCRIPTION

[0085] The disclosure provides compounds of Formula I-A, I-B, I-C, and I-D and the pharmaceutically acceptable salts thereof:

Formula I-C Formula I-D

[0086] The variables, e. g., R¹, R², R³, R⁴, R⁵, X¹, X², or Z in in Formula I or any of Formula I-A, I-B, I-C, or I-D may carry any of the definitions set forth in the SUMMARY section, or may carry any of the values set forth below.

[0087] Formula I also includes subformulae (such as Formula I-A, I-B, I-C, and I-D) in which the variables carry any of the following definitions. Any of the variable definitions below can be combined so long as a stable compound results.

[0088] Z can be absent and X¹ and X² can both be nitrogen.

[0089] Z can be absent and one of X¹ and X² can be nitrogen and while the other is carbon.

The R¹ Variable

[0090] R¹ may carry the following definitions.

[0091] (i) R¹ is hydrogen or unsubstituted CYO,alkyl.

[0092] (ii) R¹ is hydrogen.

The R² Variable

[0093] R² may carry the following definitions.

[0094] (i) R² is Ci-Cnalkyl, C2-Csalkenyl, or C2-Csalkynyl; in each Co-C4alkyl, Ci-Csalkyl, C2- Csalkenyl, or C2-Csalkynyl one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-, -C(0)0-, -OC(O), -S(0)n-, -C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the Co-C4alkyl, Ci-Cs alkyl, C2-Csalkenyl, or C2-Csalkynyl is optionally substituted with one or more substituents R¹³.

[0095] (ii) R² is Cs-Cnalkyl, optionally substituted with one or more substituents independently chosen from halogen, hydroxyl, amino, nitro, cyano, and oxo.

[0096] (iii) R² is -Co-C4alkyl(C3-C7cycloalkyl), -Co-C4alkyl(bridged C7-Ci2cycloalkyl), -Co- C4alkyl(aryl), -Co-C4alkyl(mono- or bi-cyclic heteroaryl), or -Co-C₄alkyl(4- to 7- membered

heterocycloalkyl), each of which is optionally substituted with one or more substituents independently chosen from R¹¹ and 0 or 1 substituents R¹²; in each Co-C4alkyl or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-, -C(0)0-, -OC(O), -S(0)n-, -C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the Co-C4alkyl, Ci-Cs alkyl, C2-Csalkenyl, or C2-Csalkynyl is optionally substituted with one or more substituents R¹³.

[0097] (iv) R² is -Co-C4alkyl(bridged C7-Ci2cycloalkyl) or -Co-C4alkyl(aryl), each of which is optionally substituted with one or more substituents independently chosen from R¹¹ and 0 or 1 substituents R¹²; in Co-C4alkyl one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-, -C(0)0-, -OC(O), -S(0)n-, -C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the C₀-C₄alkyl is optionally substituted by R¹³.

[0098] (v) R² is Co-C2alkyl(bridged C7-Ci2cycloalkyl), which is optionally substituted with one or more substituents independently chosen from R¹¹.

[0099] (vi) R² is adamantan-l-yl or -CH2(adamantan-l-yl), each of which is unsubstituted or substituted with halogen, hydroxyl, amino, nitro, cyano, Ci-C4alkyl, Ci-C4alkoxy, -Co-C2alkyl(mono- or di-Ci-C4alkylamino), Ci-C2haloalkyl, and Ci-C2haloalkoxy.

[0100] (vii) R² is -Co-C4alkyl(phenyl), naphthyl, benzo[d][l,3]dioxolyl, or fluorenyl, each of which is optionally substituted with one or more substituents independently chosen from R¹¹ and 0 or 1 substituents R¹²; in Co-C4alkyl one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-, -C(0)0-, -OC(O), -S(0)n-, -C(0)NR¹⁰-, -S(0)nNR¹⁰, -NR¹⁰S(O)n-, -NR¹⁰C(O)NR¹⁰, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the Co-C4alkyl is optionally substituted by R¹³.

[0101] (viii) R² is phenyl, which is optionally substituted by one or more substituents independently chosen from R¹¹.

[0102] (ix) R² is phenyl, which is substituted with one or more substituents independently chosen from halogen, hydroxyl, Ci-Cioalkyl, CVO.alkoxy, Ci-C2haloalkyl, and Ci-C2haloalkoxy.

[0103] (x) R² is phenyl, which is optionally substituted by one or more substituents

independently chosen from halogen, hydroxyl, amino, nitro, cyano, oxo, halosulfanyl, and Ci-Csalkyl, C2- Csalkenyl, and C2-Csalkynyl, wherein in each Ci-Csalkyl, C2-Csalkenyl, and C2-Csalkynyl, in the definition of R¹¹ one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(0)0-, -OC(O), or - S(0)n-, where n is 0, 1, or 2, and in which each Ci-Csalkyl, C2-Csalkenyl, or C2-Csalkynyl is optionally substituted with one or more substituents R¹³.

[0104] (xi) R² is -Co-C4alkyl(phenyl), which is optionally substituted with one or more substituents independently chosen from R¹¹ and 1 substituent R¹²; in Co-C4alkyl one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-, -C(0)0-, -OC(O), -S(0)n-, -C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the Co-C4alkyl is optionally substituted by R¹³,

where R¹² is selected from -Co-C4alkyl(C3-C7cycloalkyl), -0-Co-C₄alkyl(C₃-C₇cycloalkyl), -Co- C4alkyl(phenyl), -0-Co-C₄alkyl(phenyl), -Co-C₄alkyl(5- to 6-membered heteroaryl), -0-Co-C₄alkyl(5- to 6-membered heteroaryl), each of which is optionally substituted with one or more substituents independently chosen from halogen, hydroxyl, amino, nitro, cyano, -CHO, -COOH, oxo, Ci-C2haloalkyl, Ci-C2haloalkoxy, CVO.alkyl, CVO.alkoxy, CVO, alkyl ester, -Co-C4alkyl(mono- or di -CVO, alkyl ami no), C2-C6alkanoyl, C2-C6alkenyl, and C2-C6alkynyl.

[0105] (xii) R² is phenyl, which is substituted with one substituent R¹²; and R¹² is phenyl which is optionally substituted with one or more substituents independently chosen from halogen, hydroxyl, amino, nitro, cyano, -CHO, -COOH, oxo, Ci-C2haloalkyl, Ci-C2haloalkoxy, O-O.alkyl, CVO.alkoxy, O- C_r, alkyl ester, -Co-C4alkyl(mono- or di -CVO, alkyl ami no), C2-C6alkanoyl, C2-C6alkenyl, and C2-C6alkynyl.

The R³ Variable

[0106] R³ may carry the following definitions.

[0107] (i) R³ is hydrogen.

[0108] (ii) R³ is -Csalkyl, C2-Csalkenyl, or C2-Csalkynyl,

[0109] (iii) In O-Csalkyl, C2-Csalkenyl, or C2-Csalkynyl one or more carbon atoms is optionally replaced by O, NR¹⁰, C(0)0-, -OC(O), or -S(0)n-, where n is 0, 1, or 2, and in which the O-Cs alkyl, C2- Csalkenyl, or C2-Csalkynyl is optionally substituted with one or more substituents R¹³.

[0110] (iv) R³ is Ci-Cealkyl.

[0111] (v) R³ is CVO, alkyl optionally substituted with hydroxyl.

[0112] (vi) R³ is -Co-C4alkyl(C3-C7cycloalkyl) or -Co-C4alkyl(aryl), which is optionally substituted with one or more independently chosen R¹¹ substituents.

The R⁴ and R⁵ Variables

[0113] R⁴ and R⁵ can carry any of the following definitions

[0114] (i) R⁴ and R⁵ are both hydrogen.

[0115] (ii) One of R⁴ and R⁵ is hydrogen, and the other is chosen from halogen, hydroxyl, O- C4alkyl, Ci-C4alkoxy, Ci-C2haloalkyl, and Ci-C2haloalkoxy.

[0116] The disclosure also includes compounds of Formula I (or Formula I-A, I-B, I-C, or I-D) and pharmaceutically acceptable salts thereof, in which the variables have the following definitions.

[0117] R¹ is hydrogen or Ci-C4alkyl.

[0118] R² is C8-C12 alkyl; or R² is phenyl, which is substituted with one or more substituents independently chosen from halogen, hydroxyl, Ci-Cioalkyl, O-O.alkoxy, Ci-C2haloalkyl, and O- C2haloalkoxy, or

R² is phenyl, which is substituted with one substituent R¹²; where R¹² is phenyl which is optionally substituted with one or more substituents independently chosen from halogen, hydroxyl, amino, nitro, cyano, -CHO, -COOH, oxo, Ci-C2haloalkyl, Ci-C2haloalkoxy, O-O.alkyl, CVO.alkoxy, O- O, alkyl ester, -Co-C4alkyl(mono- or di -CVO, alkyl ami no), C2-C6alkanoyl, C2-C6alkenyl, and C2-C6alkynyl. [0119] R³ is H or Ci-C₆alkyl.

[0120] R⁴ and R⁵ are both hydrogen or one of R⁴ and R⁵ is hydrogen, and the other is chosen from halogen, hydroxyl, Ci-C4alkyl, Ci-C4alkoxy, Ci-C2haloalkyl, and Ci-C2haloalkoxy.

[0121] In this embodiment it is preferred that X¹ and X² are both N and Z is absent.

[0122] Processes for preparing compounds of a formula of the disclosure or for preparing intermediates useful for preparing compounds of Formula I or other formulas of the disclosure are provided as further embodiments. Intermediates useful for preparing compounds of Formula I or other formulas are also provided as further embodiments of the disclosure.

PHARMACEUTICAL COMPOSITIONS

[0123] The disclosure includes a pharmaceutical composition comprising a compound or salt thereof of the disclosure, together with a pharmaceutically acceptable excipient.

[0124] This disclosure provides pharmaceutical compositions comprising compounds of the Formula I. The pharmaceutical composition may comprise one or more compounds of the disclosure and pharmaceutically acceptable salts thereof, and a pharmaceutically acceptable carrier. In one embodiment, the compounds are administered as a pharmaceutical composition.

[0125] The route of administration can vary depending on the type of compound being administered. In one aspect, the compounds are administered via routes such as oral, topical, rectal, intramuscular, intramucosal, intranasal, inhalation, ophthalmic, and intravenous.

[0126] The present disclosure further provides for administration of a compound of Formula I as an immediate release or as a controlled-release formulation.

[0127] The dosage of the active compound(s) being administered will depend on the condition being treated, the particular compound, and other clinical factors such as age, sex, weight, and health of the subject being treated, the route of administration of the compound(s), and the type of composition being administered (tablet, gel cap, capsule, solution, suspension, inhaler, aerosol, elixir, lozenge, injection, patch, ointment, cream, etc.). It is to be understood that the present disclosure has application for both human and veterinary use.

[0128] Processes for preparing compounds of any of the formulas of the disclosure or for preparing intermediates useful for preparing compounds of any of the formulas of the disclosure are provided as further embodiments. Intermediates useful for preparing compounds of Formula I are also provided as further embodimentsof the disclosure.

[0129] Processes for preparing compounds of any of the formulas of the disclosure are provided as further embodiments of the disclosure and are illustrated by the following procedures in which the meanings of the generic radicals are as given above unless otherwise qualified. [0130] In one embodiment, compounds of the disclosure may be systemically administered, e.g., orally, in combination with a pharmaceutically acceptable carrier such as an inert diluent or an assimilable edible carrier. They may be enclosed in hard or soft shell gelatin capsules, may be compressed into tablets, or may be incorporated directly with the food of the patient's diet. For oral therapeutic administration, the active compound may be combined with one or more excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like. Such compositions and preparations should contain at least 0.1 % of active compound. The percentage of the compositions and preparations may, of course, be varied and may conveniently be between about 2 to about 60% of the weight of a given unit dosage form. The amount of active compound in such therapeutically useful compositions issuch that an effective dosage level will be obtained.

[0131] The tablets, troches, pills, capsules, and the like may also contain the following: binders such as gum tragacanth, acacia, corn starch or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as corn starch, potato starch, alginic acid and the like; a lubricant such as magnesium stearate; and a sweetening agent such as sucrose, fructose, lactose or aspartame or a flavoring agent such as peppermint, oil of wintergreen, or cherry flavoring may be added. When the unit dosage form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier, such as a vegetable oil or a polyethylene glycol. Various other materials may be present as coatings or to otherwise modify the physical form of the solid unit dosage form. For instance, tablets, pills, or capsules may be coated with gelatin, wax, shellac or sugar and the like. A syrup or elixir may contain the active compound, sucrose or fructose as a sweetening agent, methyl and propylparabens as preservatives, a dye and flavoring such as cherry or orange flavor. Of course, any material used in preparing any unit dosage form should be pharmaceutically acceptable and substantially non-toxic in the amounts employed. In addition, the active compound may be incorporated into sustained-release preparations and devices.

[0132] The active compound may also be administered intravenously or intraperitoneally by infusion or injection. Solutions of the active compound or its salts can be prepared in water, optionally mixed with a nontoxic surfactant. Dispersions can also be prepared in glycerol, liquid polyethylene glycols, triacetin, and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.

[0133] The pharmaceutical dosage forms suitable for injection or infusion can include sterile aqueous solutions or dispersions or sterile powders comprising the active ingredient which are adapted for the extemporaneous preparation of sterile injectable or infusible solutions or dispersions, optionally encapsulated in liposomes. In all cases, the ultimate dosage form should be sterile, fluid and stable under the conditions of manufacture and storage. The liquid carrier or vehicle can be a solvent or liquid dispersion medium comprising, for example, water, ethanol, a polyol (for example, glycerol, propylene glycol, liquid polyethylene glycols, and the like), vegetable oils, nontoxic glyceryl esters, and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the formation of liposomes, by the maintenance of the required particle size in the case of dispersions or by the use of surfactants. The prevention of the action of microorganisms can be brought about by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars, buffers or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate, and gelatin.

[0134] Sterile injectable solutions are prepared by incorporating the active compound in the required amount in the appropriate solvent with various of the other ingredients enumerated above, as required, followed by filter sterilization. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and the freeze -drying techniques, which yield a powder of the active ingredient plus any additional desired ingredient present in the previously sterile -filtered solutions.

[0135] For topical administration, the present compounds may be applied in pure form, i.e., when they are liquids. However, it will generally be desirable to administer them to the skin as compositions or formulations, in combination with a dermatologically acceptable carrier, which may be a solid or a liquid.

[0136] Useful solid carriers include finely divided solids such as talc, clay, microcrystalline cellulose, silica, alumina and the like. Useful liquid carriers include water, alcohols or glycols or water- alcohol/glycol blends, in which the present compounds can be dissolved or dispersed at effective levels, optionally with the aid of non-toxic surfactants. Adjuvants such as fragrances and additional antimicrobial agents can be added to optimize the properties for a given use. The resultant liquid compositions can be applied from absorbent pads, used to impregnate bandages and other dressings, or sprayed onto the affected area using pump-type or aerosol sprayers. Thickeners such as synthetic polymers, fatty acids, fatty acid salts and esters, fatty alcohols, modified celluloses or modified mineral materials can also be employed with liquid carriers to form spreadable pastes, gels, ointments, soaps, and the like, for application directly to the skin of the user.

[0137] Examples of useful dermatological compositions which can be used to deliver the compounds of Formula I to the skin are known to the art; for example, see Jacquet et al. (U.S. Pat. No. 4,608,392), Geria (U.S. Pat. No. 4,992,478), Smith et al. (U.S. Pat. No. 4,559,157) and Wortzman (U.S. Pat. No. 4,820,508). Useful dosages of the compounds of the disclosure can be determined by comparing their in vitro activity, and in vivo activity in animal models. Methods for the extrapolation of effective dosages in mice, and other animals, to humans are known to the art; for example, see U.S. Pat. No.

4,938,949.

[0138] Generally, the concentration of the compound(s) of the disclosure in a liquid

composition, such as a lotion, will be from about 0.1-25 wt-%, preferably from about 0.5-10 wt-%. The concentration in a semi-solid or solid composition such as a gel or a powder will be about 0.1-5 wt-%, preferably about 0.5-2.5 wt-%. The amount of the compound, or an active salt or derivative thereof, required for use in treatment will vary not only with the particular salt selected but also with the route of administration, the nature of the condition being treated and the age and condition of the patient and will be ultimately at the discretion of the attendant physician or clinician.

[0139] For example, in one embodiment relating to oral administration to humans, a dosage of between approximately 0.1 and 300 mg/kg/day, or between approximately 0.5 and 50 mg/kg/day, or between approximately 1 and 10 mg/kg/day, is generally sufficient, but will vary depending on such things as the disorder being treated, the length of treatment, the age, sex, weight, and/or health of the subject, etc. In one aspect, a unit dose is used. In one aspect, the unit dose is supplied in a syringe. The combinations of drugs can be administered in formulations that contain all drugs being used, or the drugs can be administered separately. In some cases, it is anticipated that multiple doses/times of administration will be required or useful. Additionally, for some treatment regimens, at least two compounds will be used. In one aspect, at least three compounds will be administered. The present disclosure further provides for varying the length of time of treatment.

[0140] In general, however, a suitable dose will be in the range of from about 0.5 to about 100 mg/kg, e.g., from about 10 to about 75 mg/kg of body weight per day, such as 3 to about 50 mg per kilogram body weight of the recipient per day, preferably in the range of 6 to 90 mg/kg/day, most preferably in the range of 15 to 60 mg/kg/day.

[0141] The compound is conveniently administered in unit dosage form; for example, containing 5 to 1000 mg, conveniently 10 to 750 mg, most conveniently, 50 to 500 mg of active ingredient per unit dosage form.

[0142] Ideally, when the active ingredient needs to enter circulation and be delivered via blood, the active ingredient, in one embodiment, should be administered to achieve peak plasma concentrations of the active compound of from about 0.5 to about 75 mM, preferably, about 1 to 50 mM, most preferably, about 2 to about 30 mM. This may be achieved, for example, by the intravenous injection of a 0.05 to 5% solution of the active ingredient, optionally in saline, or orally administered as a bolus containing about 1- 100 mg of the active ingredient. Desirable blood levels may be maintained by continuous infusion to provide about 0.01-5.0 mg/kg/hr or by intermittent infusions containing about 0.4-15 mg/kg of the active ingredient(s). [0143] The desired dose may conveniently be presented in a single dose or as divided doses administered at appropriate intervals, for example, as two, three, four or more sub-doses per day. The sub dose itself may be further divided, e.g., into a number of discrete loosely spaced administrations; such as multiple inhalations from an insufflator or by application of a plurality of drops into the eye.

[0144] Pharmaceutical compositions of the disclosure can further comprise additional therapeutic additives, alone or in combination (e.g., 2, 3, or 4 additional additives). Examples of additional additives include but are not limited to: (a) antimicrobials, (b) steroids (e.g., hydrocortisone, triamcinolone); (c) pain medications (e.g., aspirin, an NSAID, and a local anesthetic); (d) anti inflammatory agents; and (e) combinations thereof. Non-synthetic matrix proteins like collagen, glycosaminoglycans, andhyaluronic acid, which are enzymatically digested in the body, are useful for delivery (see U.S. Pat. Nos. 4,394,320; 4,472,840; 5,366,509; 5,606,019; 5,645,591; and 5,683,459) and are suitable for use with the present disclosure. Other implantable media and devices can be used for delivery of the compounds of the disclosure in vivo. These include, but are not limited to, sponges, such as those from Integra, fibrin gels, scaffolds formed from sintered microspheres of polylactic acid glycolic acid copolymers (PLAGA), and nanofibers formed from native collagen, as well as other proteins. The compounds of the present disclosure can be further combined with growth factors, nutrient factors, pharmaceuticals, calcium-containing compounds, anti-inflammatory agents, antimicrobial agents, or any other substance capable of expediting or facilitating bone or tissue growth, stability, and remodeling.

[0145] The compositions of this disclosure can also be combined with inorganic fillers or particles. For example for use in implantable grafts the inorganic fillers or particles can be selected from hydroxyapatite, tri-calcium phosphate, ceramic glass, amorphous calcium phosphate, porous ceramic particles or powders, mesh titanium or titanium alloy, or particulate titanium or titanium alloy.

[0146] Examples of other antimicrobial agents that can be used in the present disclosure include, but are not limited to, isoniazid, ethambutol, pyrazinamide, streptomycin, clofazimine, rifabutin, fluoroquinolones, ofloxacin, sparfloxacin, rifampin, azithromycin, clarithromycin, dapsone, tetracycline, erythromycin, cikprofloxacin, doxycycline, ampicillin, amphotericine B, ketoconazole, fluconazole, pyrimethamine, sulfadiazine, clindamycin, lincomycin, pentamidine, atovaquone, paromomycin, diclarazaril, acyclovir, trifluorouridine, foscarnet, penicillin, gentamicin, ganciclovir, iatroconazole, miconazole, Zn-pyrithione, and silver salts, such as chloride, bromide, iodide, and periodate.

[0147] In one embodiment, the compounds of the disclosure can first be encapsulated into microcapsules, microspheres, microparticles, microfibers, reinforcing fibers and the like to facilitate mixing and achieving controlled, extended, delayed and/or sustainedrelease and combined other agents or drugs. Encapsulating the biologically active agent can also protect the agent against degradation during formation of the composite of the disclosure. [0148] In another embodiment of the disclosure, the compound is controllably released into a subject when the composition of the disclosure is implanted into a subject, due to bioresorption relying on the time scale resulting from cellular remodeling. In one aspect, the composition may be used to replace an area of discontinuity in the tissue.The area of discontinuity can be the result of trauma, a disease, disorder, or condition, surgery, injury, etc.

[0149] As used herein, an "instructional material" includes a publication, a recording, a diagram, or any other medium of expression which can be used to communicate the usefulness of the composition of the disclosure for its designated use. The instructional material of the kit of the disclosure may, for example, be affixed to a container which contains the composition or be shipped together with a container which contains the composition. Alternatively, the instructional material may be shipped separately from the container with the intention that the instructional material and the composition be used cooperatively by the recipient.

[0150] The method of the disclosure includes a kit comprising a compound identified in the disclosure and an instructional material which describes administering the compound or a composition comprising the compound to a a subject. This should be construed to include other embodiments of kits that are known to those skilled in the art, such as a kit comprising a (preferably sterile) solvent suitable for dissolving or suspending the composition of the disclosure prior to administering the compound to a subject. Preferably the subject is a human.

[0151] In accordance with the present disclosure, as described above or as discussed in the Examples below, there can be employed conventional chemical, cellular, histochemical, biochemical, molecular biology, microbiology, and in vivo techniques which are known to those of skill in the art.

Such techniques are explained fully in the literature.

[0152] Without further description, it is believed that one of ordinary skill in the art can, using the preceding description and the following illustrative examples, make and utilize the compounds of the present disclosure.

METHODS OF TREATMENT

[0153] Mitochondria regulate cellular metabolism and play an important role in the pathogenesis of some of the most prevalent human diseases including obesity, cancer, diabetes, neurodegeneration, and heart disease. The compounds of the disclosure, including are useful for treating and preventing these diseases and disorders and others described herein, as well as others where a mitochondrial uncoupler is useful.

[0154] Many anti-diabetes drugs such as insulin-sensitizers promote glucose clearance from the blood by effectively‘pushing’ glucose into nutrient overloaded tissues; however, in contrast to this approach our strategy is aimed at reducing cellular nutrient stores so that tissues will‘pull’ glucose from the circulation. The present method is modeled after exercise and calorie restriction interventions which also reduce cellular nutrient stores to improve glycemia and insulin sensitivity. The proof of principle is validated in humans treated with the mitochondrial uncoupler 2,4-dinitrophenol (DNP). DNP decreases adiposity and improves metabolism in humans; however, it also has a very narrow therapeutic window and was removed from FDA approval in 1938. Other anti-diabetes drugs including agonists of thyroid hormone and inhibitors of l l-b hydroxysteroid dehydrogenase type 1 have off-target effects of increased energy expenditure that may mediate some of the protective effects of these compounds. Nevertheless, there are no drugs have been specifically targeted for increased energy expenditure.

[0155] In one embodiment, a compound of the disclosure is useful for treating disease, disorders, and conditions which are associated with defects in mitochondrial function or which can be treated with drugs or agents that act as uncoupling agents. The methods can comprise administering to a subject in need thereof a pharmaceutical composition comprising an effective amount of compound of Formula I, or a salt thereof as a first therapeutic agent, together with a pharmaceutically acceptable carrier, and optionally with at least one additional therapeutic agent.

[0156] In one embodiment, the present disclosure provides compositions and methods for increasing oxygen consumption, decreasing cellular reactive oxygen species, depolarizing a mitochondrial inner membrane, and increasing oxygen consumption rate without donating electrons to the electron transport chain using a mitochondrial uncoupler, said method comprising contacting a cell or

mitochondria with a composition comprising at least one compound of the disclosure and optionally an additional therapeutic agent.

[0157] For example, it is disclosed herein that the mitochondrial uncoupling agents of this disclosure both prevent and reverse body fat mass increases in mice fed a high fat and high sugar Western diet. Apart from body fat, the mitochondrial uncoupling agents decrease insulin levels, which is important because it corrects hyperinsulinemia, improves glucose tolerance, and protect against diet- induced glucose tolerance. It is also disclosed herein that administration of the mitochondrial uncoupling agents reverses insulin resistance, including diet-induced insulin resistance, and restores insulin sensitivity index. Therefore, the compounds of the disclosure are useful for preventing and treating diabetes. It is also disclosed that compounds of the disclosure decrease liver fat, thus providing a treatment for fatty liver disease. It is disclosed herein that a compound of the disclosure can prevent weight gain without altering food intake and can prevent di-t-induced fat accumulation. Compounds of the disclosure are also useful for reversing diet-induced weight or fat gain and can reverse diet-induced fat gain and fatty liver.

[0158] Reactive oxygen species generated during respiration contribute to biological damage over time, causing mutations and other biological changes that lead to cancer, aging, and decreased lifespan. Mitochondrial uncoupling decreases the production of reactive oxygen species, potentially lowering the risk of cancer, decreasing the effects of aging, and increasing lifespan. Mitochondrial uncouplers reverse or interfere with many aspects of cancer metabolism and are therefore effective in a broad range of cancer types. For example, mitochondrial uncouplers are effective in treatment of cancers with impaired p53 expression or activity (https ://www.nature.com/articles/s41467 -018-05805 -1 ) such as certain breast and ovarian cancers, Ras mutant cancers (https://www.cell.com/molecular-cell/pdf/Sl097- 2765(l5^')00004-0.pdf). and/or beta-catenin mutant cancers

(https://www.ncbi.nlm.nih.gov/pubmed/28l07588^'). Mitochondrial uncouplers are demonstrated to treat adrenocortical carcinoma (http://clincancerres.aacriournals.org/content/clincanres/early/20l6/02/l2/l078- 0432.CCR-l5-2256.full.pdf) melanoma (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833689/^'), primary colon cancer (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056247/^') and metastasis to distant organs including the liver (https://www.nature.com/articles/s41419-017 -0092-6^').

[0159] A compound of the disclosure may exhibit at least one of the following properties or activities: energy expenditure agonist, mitochondrial uncoupler, antioxidant, increases oxygen consumption, depolarizes the mitochondrial inner membrane, stimulates respiration in isolated mitochondria, increases or stimulates oxygen consumption without donating electrons to the electron transport chain, lacks protonophore activity at the plasma membrane, decreases reperfusion-induced mitochondrial oxidative stress, decreases cellular reactive oxygen species, improves glucose tolerance, provides protection from high fat induce glucose tolerance, activates AMPK without depletion of ATP, prevents, reverses or treats insulin resistance, prevents, reverses or treats hyperinsulinemia, prevents, reverses or treats hyperlipidemia, improves blood lipid profiles, improves leanness, improves insulin sensitivity, protects from ischemic-reperfusion injury, and is less toxic than other mitochondrial inhibitors. In one embodiment, a compound of the disclosure has two or more of these properties. In one embodiment, a compound of the disclosure has three or more of these properties. In one embodiment, a compound of the disclosure has four, five, six, seven, eight, nine, ten, eleven, twelve, or more of these properties. In one embodiment, a compound of the disclosure has one, two, three, four, five, six, seven, eight, nine, or ten of these properties.

[0160] Compounds of the disclosure can be administered to a subject at various times, dosages, and more than once, depending on, for example, the age, sex, health, and weight of the subject, as well as on the particular disease, disorder, or condition to be treated or prevented. In one aspect, a compound is administered at a dosage ranging from about 0.1 mg/kg to about 500 mg/kg body weight. In another aspect, the compound is administered at a dosage ranging from about 0.5 mg/kg to about 100 mg/kg body weight or about 0.5 mg/kg to about 25 mg/kg body weight. In yet another aspect, the compound is administered at a dosage ranging from about 1.0 mg/kg to about 50 mg/kg body weight. In one aspect, about 3.0 mg/kg is administered. In another aspect, about 5.0 mg/kg is administered. In one aspect, the dose is selected from 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 2.0, 3.0, 4.0, 5.0, 6.0, 7.0, 8.0, 9.0, 10,

11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 34, 35, 36, 37, 38, 39,

40, 41, 42, 43, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68,

69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96,

97, 98, 99, 100, 110, 120, 130, 140, 150, 160, 170, 180, 190, 200, 300, 400, and 500 mg/kg body weight, as well as all fractions, decimals, and integers in the range of numbers listed. In another aspect, the compound is administered as a unit dose ranging from about 10 mg to about 500 mg/unit dose.

[0161] In one aspect, a compound is administered to a subject more than once. In one aspect, the compound is a mitochondrial protonophore uncoupler lacking protonophore activity at the plasma membrane.

[0162] In one aspect the disclosure provides a method of treating or preventing a condition responsive to mitochondrial uncoupling, comprising administering a therapeutically effective amount of a compound Formula I or salt thereof to a patient in need of such treatment.

[0163] In one aspect, the disease, disorder or condition associated with a defect in mitochondria function is selected from the group consisting of obesity, ischemia reperfusion injury, hyperinsulinemia, hyperlipidemia, glycemia, glucose tolerance, insulin sensitivity, adiposity, insulin resistance, obesity, diabetes, cancer, neurodegeneration, heart disease, renal disease, heart failure, Parkinson’s disease, traumatic brain injury, stroke, aging, and disorders standing to benefit from increased energy expenditure. In one aspect, the compound is a mitochondrial uncoupler.

[0164] In one aspect the condition responsive to mitochondrial uncoupling is obesity, type II diabetes, fatty liver disease, insulin resistance, multiple sclerosis, cancer, Huntington’s disease,

Alzheimer’s dementia, Parkinson’s disease, ischemia reperfusion injury, heart failure, non-alcoholic fatty liver disease (NALFD), or non-alcoholic steatohepatitis (NASH).

[0165] The disclosure also includes a method of increasing lifespan comprising administering an effective amount of a compound of Formula I, or salt thereof, to a human or non-human animal.

Increasing lifespan can be via delaying aging by delaying the onset of age-related disease, or age related changes, including neurodegenerative diseases, an age related cognitive decline, or an age-related decrease in motorneuron responses. The disclosure includes a method of increasing lifespan by delaying the onset of diseases associated with aging, comprising administering an effective amount of a compound of Formula I, or salt thereof, to a human or non-human animal.

[0166] The disclosure includes a method of regulating glucose homeostasis or insulin action in a patient comprising administering a therapeutically effective amount of a compound or salt of any one of Formula I to the patient. [0167] The disclosure includes a method of treating hyperlipidemia, glycemia, glucose tolerance, insulin sensitivity, adiposity, insulin resistance, obesity, or diabetes in a patient comprising administering a therapeutically effective amount of a compound of Formula I to the patient.

[0168] One of ordinary skill in the art will appreciate that not all configurations need to be effective or as effective as other compounds of the genus based on the teachings disclosed herein.

[0169] The disclosure is now described with reference to the following Examples and

Embodiments. Without further description, it is believed that one of ordinary skill in the art can, using the preceding description and the following illustrative examples, make and utilize the present disclosure and practice the claimed methods. The following working examples therefore, are provided for the purpose of illustration only and specifically point out the preferred embodiments of the present disclosure, and are not to be construed as limiting in any way the remainder of the disclosure. Therefore, the examples should be construed to encompass any and all variations which become evident as a result of the teaching provided herein.

EXAMPLES GENERAL METHODS

[0170] The following starting materials and general procedures are used in synthetic examples that follow.

In all synthetic examples room temperature (rt) is about 21 °C.

NMR Solvent Reference: (CD3)2CO (2.05/29.84 ppm); (CD3)2SO (2.50/39.52 ppm).

NMR Abbreviations: aq. = aqueous, app = apparent, br = broad, s = singlet, d = doublet, t = triplet, q = quartet, p = pentet. * means rotamers.

PYRAZINE ANALOGS GENERAL PROCEDURE 3-A.

[0171] To anhydrous THF (25 mL) was added sodium hydride (1.5 equiv., 60 percent dispersion) and allowed to stir for 5 min. Benzyl alcohol (1.0 equiv.) in anhydrous THF (15 mL) was added dropwise over a minute and allowed to stir for 30 min. 2,3-Dichloropyrazine (1.0 equiv.) in THF (10 mL) was added and the reaction was allowed to stir at room temperature for 2 h (TLC monitoring) and the reaction was quenched slowly with isopropanol. The solvent was evaporated under reduced pressure and the product purified via silica chromatography (2.5% ethyl acetate:hexanes.)

GENERAL PROCEDURE 3-B.

[0172] A sealed vial was charged with Pd2dba3 (45.8 mg, 10 mol percent), Xantphos (67.21 mg, 10 mol percent), 2-(benzyloxy)-3-chloropyrazine (1.162 mmol) and K2CO3 (2.323 mmol). The flask was then evacuated and backfilled with argon 3X. Deoxygenated anhydrous dioxane (4 mL) was added through the septum, with the requisite aniline (1.278 mmol). The mixture stirred at 110 °C for 16 h and then allowed to cool to room temperature. After cooling, the solid material was filtered off and washed with ethyl acetate. The solvent was evaporated, and methanol (4 mL) was added. The round bottom flask was flushed with nitrogen gas for 5 min. Pd/C 10% (62 mg) was added and the mixture was stirred under a hydrogen balloon for 1.5 h at room temperature. The reaction was then filtered through a Celite plug washing with ethyl acetate, concentrated under reduced pressure, and purified via silica gel

chromatography (ethyl acetate:hexanes 40%-55%) to provide the desired product (109 mg 37%).

GENERAL PROCEDURE 3-C.

[0173] To a mixture of 3-amino-6-bromopyrazin-2-ol (3-20) (100 mg, 0.31 mmol), 4- dimethylaminopyridine (4 mg, 0.03 mmol) and triethylamine (47 mg, 0.47 mmol) in dry dichloromethane (2 mL) was added o-fluorobenzoyl chloride (60 mg, 0.38 mmol) in dry DCM (1 mL) via syringe. The resulting mixture was stirred at room temperature for 16 h. The solvent was concentrated under reduced pressure. The residue was dissolved in methanol (5 mL) and potassium carbonate (1 equiv.) was added. The mixture was refluxed for 2 h, concentrated under reduced pressure, dissolved in THF, filtered, and concentrated under reduce pressure to afford the desired compound.

EXAMPLE 1. SYNTHESIS OE 2-(BENZYT .OX Y)-3-C.HT .OR OPYR AZTNE (3-1)

[0175] Compound 3-2 was synthesized by general procedure 3-B to yield 3-2 as brown solid. (20% Yield). HRMS (ESL): Calc’d for C H N O+ [M+H] + : 280.2383 Found: 280.2385

EXAMPLE 3. SYNTHESIS OF 3-((4-DEC.YT .PHENYT .) AMINOJPYR AZTN-2-OT . (3-3)

[0176] Compound 3-3 was synthesized by general procedure 3-B to yield 3-3 as an off white solid. (33% Yield). Ή NMR (400 MHz, Chloroform-* d 12.16 (s, 1H), 8.04 (s, 1H), 7.68 (d, 7 = 8.1 Hz, 2H), 7.17 (d, 7 = 8.1 Hz, 2H), 7.09 (d, 7 = 4.4 Hz, 1H), 6.67 (d, 7 = 4.4 Hz, 1H), 2.58 (t, 7 = 7.7 Hz, 2H), 1.60 (p, 7 = 7.2 Hz, 2H), 1.37 - 1.24 (m, 14H), 0.88 (t, 7 = 6.6 Hz, 3H). ¹³C NMR (101 MHz, Chloroform- d) d 153.11, 148.87, 138.02, 136.53, 129.03, 123.44, 119.37, 114.03, 35.53, 32.04, 31.73, 29.77, 29.76, 29.67, 29.48, 29.42, 22.83, 14.27. HRMS (ESI⁺): Calc’d. for C20H30N3O+ [M+H] + : 328.2383 Found: 328.2383.

EXAMPLE 4. SYNTHESIS OF 3-((PERET J IOROPHENYT .) AMTNO)PYR AZTN-2-OT . (3-4)

[0177] Compound 3-4 was synthesized by general procedure 3-B to yield 3-4 as a yellow solid. (29% Yield). Ή NMR (400 MHz, Acetone-*) d 11.13 (s, 1H), 8.42 (s, 1H), 6.91 (d, 7 = 4.4 Hz, 1H), 6.81 (d, 7 = 4.5 Hz, 1H). ¹⁹F NMR (376 MHz, Acetone-*) d -145.72 - -146.43 (m), -161.22 (t, 7 = 21.1 Hz), -166.08 (dd, J = 21.1, 16.4 Hz). HRMS (ESI⁺): Calc’d. for C10H5F5N3O+ [M+H] + : 278.0347 Found: 278.0335.

EXAMPLE 5. SYNTHESIS OF 3-((2-ET J TOR OPHENYT .) AMTNO)P YR AZTN-2-OT . (3-5)

[0178] Compound 3-5 was synthesized by general procedure 3-B to yield 3-5 as an off white solid. (32% Yield). Ή NMR (400 MHz, Acetone-*) d 10.98 (s, 1H), 8.79 - 8.68 (m, 1H), 8.42 (s, 1H), 7.27 - 7.14 (m, 2H), 7.08 - 7.00 (m, 1H), 6.97 (d, 7 = 4.5 Hz, 1H), 6.91 (d, 7 = 4.5 Hz, 1H). ¹⁹F NMR (376 MHz, Acetone-*) d -134.06 - -134.15 (m, 1F). ¹³C NMR (101 MHz, Acetone-*) d 153.35 (d, 7 = 241.9 Hz), 149.73, 139.10, 136.51, 125.34 (d, 7 = 3.9 Hz), 123.36 (d, 7 = 7.7 Hz), 121.50, 120.70 (d, 7 = 1.6 Hz), 116.91, 115.37 (d, 7 = 19.1 Hz). HRMS (ESI⁺): Calc’d. for C10H9FN3O+ [M+H] + : 206.0724 Found: 206.0716

EXAMPLE 6. SYNTHESIS OF 3-((4-(TRTET J JOROMETHOXY)PHENYT .) AMTNO)P YR AZTN-2-OT . (3-6)

[0179] Compound 3-6 was synthesized by general procedure 3-B to yield 3-6 as an off white solid. (12% Yield). Ή NMR (400 MHz, Acetone-*) d 10.90 (s, 1H), 8.77 (s, 1H), 8.21 - 8.13 (m, 2H), 7.33 - 7.26 (m, 2H), 6.94 (d, / = 4.4 Hz, 1H), 6.87 (d, / = 4.4 Hz, 1H). ¹⁹F NMR (376 MHz, Acetone-*) d -58.87 (s, 3F). ¹³C NMR (101 MHz, Acetone-*) d 152.40, 150.03, 144.26 (q, / = 2.1 Hz), 121.55 (q, J = 255Hz), 121.50, 116.60. HRMS (ESI⁺): Calc’d. for C11H9F3N3O2+ [M+H] + : 272.0641 Found: 272.0627. EXAMPLE 7. SYNTHESIS OF 3-((3 ,5-RTS (TRTET I IOROMETHYT JPHF.NYI .) AMTNO)PYR AZTN-2-OT . (3-7)

[0180] Compound 3-7 was synthesized by general procedure 3-B to yield 3-7 as an off yellow solid. (36% Yield). Ή NMR (400 MHz, Acetone-*) d 11.02 (s, 1H), 9.18 (s, 1H), 8.86 - 8.79 (m, 2H), 7.68 - 7.56 (m, 1H), 7.02 (d, / = 4.5 Hz, 1H), 6.97 (d, / = 4.5 Hz, 1H). ¹⁹F NMR (376 MHz, Acetone-*) d -63.53. ¹³C NMR (101 MHz, Acetone-*) d 152.16, 150.03, 142.83, 132.33 (q, J = 33.2 Hz), 125.94 (q, / = 272.3 Hz), 121.06, 119.87 - 119.11 (m), 117.92, 115.54 - 115.05 (m). HRMS (ESI⁺): Calc’d. for C12H8F6N3O+ [M+H] + : 324.0566 Found: 324.0556.

EXAMPLE 8. SYNTHESIS OF 3-((4-(TRTET .I IOROMETHYT OPHENYT .) AMTNO)PYR AZTN-2-OT . (3-8)

[0182] Compound 3-9 was synthesized by general procedure 3-B to yield 3-9 a brown solid. (35% Yield). ¾ NMR (400 MHz, Acetone-*) d 10.86 (s, 1H), 8.87 (s, 1H), 8.70 - 8.39 (m, 1H), 8.31 - 8.15 (m, 1H), 7.54 (t, 7 = 8.0 Hz, 1H), 7.42 - 7.23 (m, 1H), 6.98 (d, 7 = 4.4 Hz, 1H), 6.91 (d, 7 = 4.5 Hz, 1H). ¹⁹F NMR (376 MHz, Acetone-*) d -63.13 (s, 3F). ¹³C NMR (101 MHz, Acetone-*) d 152.36 (d, 7 = 2.7 Hz), 150.10, 141.70, 131.24 (d, 7 = 31.6 Hz), 130.33, 125.40 (d, 7 = 271.3 Hz), 123.21 (d, 7 = 1.5 Hz), 121.42, 119.14 (q, 7 = 4.2 Hz), 116.98, 115.93 (q, 7 = 3.9 Hz).; HRMS (ESI⁺): Calc’d. for CnH₉F₃N₃0+ [M+H] + : 256.0692 Found: 256.0687.

EXAMPLE 10. SYNTHESIS OF 3-((3'-METHOXY-[1 ,1 '-RTPHENYT.]-3-YT.)AMTNO)PYRAZTN-2-OT. (3-10)

[0183] Compound 3-10 was synthesized by general procedure 3-B to yield 3-10 as an off brown solid. (30% Yield). ¾ NMR (500 MHz, DMSO-*) d 11.97 (s, 1H), 9.20 (s, 1H), 8.17 - 8.02 (m, 2H), 7.69 - 7.53 (m, 2H), 7.35 (t, 7 = 7.9 Hz, 1H), 7.26 - 7.20 (m, 1H), 7.18 (t, 7 = 2.1 Hz, 1H), 6.92 (d, 7 = 4.3 Hz, 1H), 6.89 (dd, 7 = 8.2, 2.5 Hz, 1H), 6.82 (d, 7 = 4.3 Hz, 1H), 3.82 (s, 3H). HRMS (ESI⁺): Calc’d for C_I7H_I6N₃0₂+ [M+H] + : 294.1237 Found: 294.1236

EXAMPLE 11. SYNTHESIS OF 3-((4'-ELIIORO-[1 , 1 '-RTPHENYL]-4-YL)AMTNO)PYRAZTN-2-OL (3-11)

[0184] Compound 3-11 was synthesized by general procedure 3-B to yield 3-11 as an off brown solid. (16% Yield). ¾ NMR (400 MHz, DMSO-*) d 11.95 (s, 1H), 9.18 (s, 1H), 8.18 - 7.91 (m, 2H), 7.79 - 7.59 (m, 2H), 7.61 - 7.42 (m, 2H), 7.32 - 7.14 (m, 2H), 6.90 - 6.84 (m, 1H), 6.81 - 6.72 (m, 1H). ¹⁹F NMR (376 MHz, DMSO-*) d -116.47 (tt, 7 = 8.9, 5.4 Hz, 1F). ¹³C NMR (101 MHz, DMSO-*) d 162.70, 160.28, 150.19 (d, 7 = 252.5 Hz), 139.43, 136.44 (d, 7 = 3.0 Hz), 132.52, 128.04 (d, 7 = 8.0 Hz), 126.60, 120.51, 119.49, 115.63 (d, 7 = 21.9 Hz). HRMS (ESI⁺): Calc’d. for Ci₆H₁₃FN₃0+ [M+H] + : 282.1037 Found: 282.1037.

EXAMPLE 12. SYNTHESIS OF 3-(BENZYLOXY)-2-CHLOROPYRIDINE (3-12)

[0185] NaH (0.37 g, 9.26 mmol 60% dispersion) was added to a solution of 2-chloropyridin-3-ol (1.00 g, 7.72 mmol) in dry DMF (20 ml) at 0 °C. The mixture was stirred for 30 min and benzyl bromide (1.10 ml, 9.26 mmol) was added to the mixture. The mixture was then stirred at room temperature overnight. Upon completion, the mixture was poured into ice-water, and extracted with ethyl acetate 3X. The combined organic layers were washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to yield 3-(benzyloxy)-2-chloropyridine 3-12 as a grey solid. (83% Yield). ¹ H NMR (400 MHz, Chloroform- d) d 8.02 - 7.90 (m, 1H), 7.45 - 7.28 (m, 6H), 7.16 - 7.09 (m, 1H), 5.15 (s, 2H).

EXAMPLE 13. SYNTHESIS OF 2-((4-(TRIFLUOROMETHYL)PHENYL)AMINO)PYRIDIN-3-OL (3-13)

[0186] Compound 3-13 was synthesized by general procedure 3-B to yield 3-13 as a greyish solid. (62% Yield). Ή NMR (400 MHz, Acetone-*) d 9.21 (s, 1H), 8.26 - 8.08 (m, 2H), 7.96 (s, 1H), 7.88 - 7.68 (m, 1H), 7.66 - 7.48 (m, 2H), 7.20 - 7.09 (m, 1H), 6.84 - 6.64 (m, lH).¹⁹F NMR (376 MHz, Acetone-*) d -61.81 (s, 3F). ¹³C NMR (126 MHz, Acetone-*) d 146.45, 146.06, 141.11, 138.39, 126.54 (q, 7 = 3.8 Hz), 125.94 (q, 7 = 270.0 Hz), 121.98 (q, 7 = 32.2 Hz), 120.36, 118.40, 116.50. HRMS (ESI⁺): Calc’d.. for (C_I2H_IOF₃N₂0)+ : 255.0740 Found: 255.0775.

EXAMPLE 14. SYNTHESIS OF 2-((3-(TRIFLUOROMETHYL)PHENYL)AMINO)PYRIDIN-3-OL (3-14)

[0187] Compound 3-14 was synthesized by general procedure 3-B to yield 3-14 as a greyish solid. (59% Yield). Ή NMR (400 MHz, Acetone-*) d 8.42 (s, 1H), 8.10 - 7.98 (m, 1H), 7.94 - 7.80 (m, 1H), 7.80 - 7.50 (m, 3H), 7.35 - 7.28 (m, 1H), 7.26 - 7.16 (m, 1H), 6.96 - 6.78 (m, 1H). ¹⁹F NMR (376 MHz, Acetone-*) d -63.05 (s, 3F). HRMS (ESI ): Calc’d. for (Ci₂H₈F₃N₂0-) [M-H] - : 253.0594 Found: 253.0637

EXAMPLE 15. SYNTHESIS OF 2, 3 -DTC.HT .OR O-5 -TODOP YR AZTNE (3-15)

[0188] Compound 3-15 was prepared according to a reported method (Bisballe N. et al., Eur. J. Org. Chem. 2018, 3904-3913) described as follows. A solution of LiTMP [prepared by adding uBuLi (2.5M solution in hexanes, 70.48 mmol, 1.5 equiv., 28.0 mL) to a stirred, cooled (0 °C) solution of freshly distilled TMP (70.48 mmol, 1.5 equiv., 11.9 mL) in anhydrous THF (50 mL) and stirring for 5 min] cooled to approximately -30 °C (ACN + CO2 (s) bath) was slowly transferred to a solution of the 2,3- dichloropyrazine (46.99 mmol, 1.0 equiv., 7.00 g) and ZnCL· TMEDA (46.99 mmol, 1.0 equiv., 11.86 g) in anhydrous THF (50 mL) at the same temperature. The resulting mixture was stirred for 15 min at -30 °C and then cooled down to -78 °C (acetone + CO2 (s) bath). A solution of L (70.48 mmol, 1.5 equiv., 17.89 g) in THF (60 mL) was introduced to the reaction mixture and it was stirred for 1.5 h at room temperature. The reaction was quenched with sat. aq. Na2S2C>3 (10 mL) and extracted with EtOAc (3x20 mL). The combined organic layers were washed with brine (10 mL), and dried with Na2S04- The solvent was removed under reduced pressure. The crude product was purified by flash column chromatography on silica gel to yield 3-15 (9.25 g, 72%) as an, off-white solid: R_/= 0.62 (hex : EtOAc 15: 1); 'H NMR (CDCL, 400 MHz) d 8.53 (1H, s); ¹³C NMR (125 MHz, CDCL) d 149.86, 147.57, 147.42, 111.03; HRMS (ESI-TOF) m/z calc’d. for C₄HCLIN₂ [M⁺] 273.8560; found 273.8275.

EXAMPLE 16. SYNTHESIS OF 2,3-DTCHT .ORO-5-(TRTET .I IOROMETHYT .)PYR AZTNE (3-16)

[0189] A mixture of compounds 3-15 (9.97 mmol, 1 equiv., 2.74 g), KF (13.96 mmol, 1.4 equiv., 0.81 g) and Cul (15.95 mmol, 1.6 equiv., 3.04 g) were sealed in a high-pressure tube with a septum- containing cap, evacuated, and refilled with N2 three times. Then DMSO (6 mL) and TMSCF3 (19.94 mmol, 2 equiv., 2.94 mL) were added via syringe and the mixture was stirred at 70 °C for 4 hours. After cooling to rt, the solution was diluted with water and extracted with Et₂0 (5x20 mL). Combined organic layers were washed with water, dried with MgSCL, filtered and slowly evaporated without additional heating. Brown slurry product 3-16 (1.95 g, 91%) was used without further purification to yield: R_/ = 0.41 (hex : EtOAc 15: 1); ¾ NMR (CDCL, 400 MHz) d 9.21 (1H, s); ¹⁹F NMR (CDCL, 376 MHz) d -67.25; HRMS (ESI-TOF) = calc’d. for C5HCI2F3N2 [M⁺] 215.9; found 215.9.

EXAMPLE 17. SYNTHESIS OF 3-(BENZYLOXY)-2-CHLORO-5-(TRIFLUOROMETHYL)PYRAZINE (3-17)

[0190] A round bottom flask was charged with anhydrous THF (5 mL) and NaH (90% in mineral oil, 2.05 mmol, 1.2 equiv., 55 mg). To this stirred mixture, a solution of BnOH (2.05 mmol, 1.2 equiv., 0.21 mL) in anhydrous THF (5 mL) was added. The mixture was stirred at rt for 30 minutes until the bubbling has stopped and then a solution of 3-16 (1.71 mmol, 1 equiv., 370 mg) in anhydrous THF (5 mL) was added. The reaction was then stirred overnight at rt. After quenching with /^'RiΌH, the reaction mixture was extracted between Et₂0 and water. The combined organic layers were washed with brine and dried with MgSCh, filtered, evaporated under vacuum and purified by column chromatography to yield 3- 17 (218 mg, 44%) as a white solid: R_/= 0.60 (hex : EtOAc 15:1, blue spot); ¹ H NMR (CDCh, 400 MHz) d 8.96 (1H, s), 7.53 - 7.44 (2H, m), 7.43 - 7.30 (3H, m), 5.54 (2H, s); ¹⁹F NMR (CDCl₃, 376 MHz) d - 66.70; HRMS (ESI-TOF) = calc’d. for C12H8CIOF3N2 [M⁺] 288.0277; found 288.8559.

EXAMPLE 18. SYNTHESIS OF 3-(BENZYLOXY)-/V-(4-(TRIFLUOROMETHOXY)PHENYL)-5- (TR TFT .t TOR OMETH YT .)PYR AZTN-2-AMTNE (3-18)

[0191] A vial with a stir bar was charged with Pd(dba)2 (5.2 pmol, lmol%, 2.99 mg), XPhos (5.2 pmol, 2 mol%, 4.95 mg), 3-17 (0.52 mmol, 1 equiv., 150.0 mg), aniline derivative (0.62 mmol, 1.2 equiv., 0.84 mL) and zBuONa (0.73 mmol, 1.4 equiv., 69.9 mg) and sealed with a septum containing cap.

The vial was evacuated and flushed with N2 three times and heated at 110 °C for 48 h. After completion of reaction, the tube was allowed to cool to room temperature and the mixture was immediately purified by silica gel column chromatography to yield 3-18 (12.0 mg, 6%) as a yellow solid: R_/= 0.15 (hex : EtOAc 15:1). ¾ NMR (CDCl₃, 400 MHz) d 7.87 (1H, br s), 7.73 (2H, d, / = 9.1 Hz), 7.44 - 7.37 (5H, m), 7.25 (1H, s), 7.17 (2H, d, / = 8.3 Hz), 5.51 (2H, s); ¹⁹F NMR (CDCl₃, 376 MHz) d -58.19,

-67.51 ; HRMS (ESI-TOF) = calc’d. for C19H13F6N3O2 [M+H⁺] 430.0912; found 430.0890.

EXAMPLE 19. SYNTHESIS OF 3-((4-(TRIFLUOROMETHOXY)PHENYL)AMINO)-6- (TRTET .1 IOROMETHYT .)PYR AZTN-2-OT . (3-19)

[0192] Pd(OH)2 (0.20 mmol, 20.0 mg) and 3-18 (10 pmol, 1 equiv., 5.0 mg) were dissolved in EtOAc (1 mL) in a round bottom flask with a stir bar. Flask was degassed 5 times and filled with ¾ and the reaction mixture was stirred overnight. The reaction mixture was then filtered through a Celite pad, washed with MeOH and concentrated. The mixture was purified by silica gel column chromatography to yield 3-19 (3.1 mg, 90%) as a colorless solid: R_/ = 0.11 (hex : EtOAc 15:1). 'H NMR ((CD₃)₂CO, 400 MHz) d 8.97 (1H, br s), 8.18 (2H, d, / = 9.2 Hz), 7.45 (1H, s), 7.34 (2H, d, / = 9.2 Hz); ¹⁹F NMR ((CD₃)₂CO, 376 MHz) d = -58.89, -68.70; HRMS (ESI-TOF) = calc’d. for 0i₂H₇E₆N₃0₂ [M+H⁺] 340.0442; found 340.0535.

EXAMPLE 20. SYNTHESIS OF 3-AMINO-6-RROMOPYRAZIN-2-OL (3-20)

[0193] In a round-bottom flask, to 5-bromo-3-chloropyrazin-2-amine (1.00 g) was added potassium hydroxide (1.346 g, 5 equiv) in water (15 mL) and the resulting mixture was stirred at 100 °C for 16 h. The solution was allowed to cool to room temperature and then acidified with HC1 (1 M) to pH 1 where a white precipitate formed. The solid was filtered, washed with water, and collected to afford (3- 20) as a white solid (720 mg, 79%). ¾ NMR (400 MHz, DMSO-dg) d 12.41 (s, 1H), 6.97 (s, 1H), 6.58 (s, 2H).

EXAMPLE 21. SYNTHESIS OF N-(5 -RR OMO-3 -HYDR OX YP YR AZTN-2- YT .) -3 -ET ,T TOR ORENZ AMTDE (3-21)

[0194] Compound 3-21 was synthesized by general procedure 3-C as a tan solid (11% yield). 'H NMR (400 MHz, DMSO-dg) d 10.53 (s, 1H), 7.99 (s, 1H), 7.79 - 7.72 (m, 1H), 7.69 (dt, / = 9.9, 2.1 Hz, 1H), 7.53 (td, / = 8.0, 5.8 Hz, 1H), 7.42 (td, J = 8.4, 2.6 Hz, 1H) -OH not visible. ¹⁹F NMR (376 MHz, DMSO-dg) d -112.49 (td, J = 9.3, 6.1 Hz, IF). Calc’d. for CnH₇FN₃0₂ ⁺ [M+H]⁺ : 311.9739, Observed: 311.9748.

EXAMPLE 22. SYNTHESIS OF N-(5 -RR OMO-3 -HYDR OX YP YR AZTN-2- YT .) -2-ET ,I TOR ORENZ AMTDE (3-22)

[0195] Compound 3-22 was synthesized by general procedure 3-C as a tan solid (40% yield). 'H NMR (400 MHz, DMSO d₆) d 13.13 (s, 1H), 10.34 (d, J = 3.7 Hz, 1H), 7.91 (s, 1H), 7.73 (td, J = 7.5, 1.7 Hz, 1H), 7.65 - 7.57 (m, 1H), 7.38 - 7.30 (m, 2H). ¹⁹F NMR (376 MHz, DMSO- d₆) d -113.49 (s, IF). Calc’d. for C_nH₇FN₃0₂ ⁺ [M+H]⁺ : 311.9739, Observed: 311.9748.

EXAMPLE 23. 5-(4-(TRTET .I TOROMETHYT OPHENYT .)PYR AZTN-2- AMTNE (3-23)

[0196] A sealed vial was charged with Pd dba (158 mg, 3 mol percent), triphenyl phosphine (181 mg, 12 mol percent), 5-bromopyrazin-2-amine (1.00 g, 5.75 mmol), (4-

(trifluoromethyl)phenyl)boronic acid (1.20 g, 5.75 mmol) and Na CC (1.83 g, 17.2 mmol). The flask was then evacuated and backfilled with argon 3X. Degassed dioxane: water (22 mL, 2:1) was added through the septum and the mixture was stirred at 110 °C for 16 h. The reaction was allowed to cool to room temperature, filtered, and concentrated under reduced pressure. The residue was then purified via silica gel chromatography (ethyl acetate: hexanes) to afford 3-23 as a yellow solid (818 mg, 60%). GCMS (El): Calc’d for CnH₈F₃N₃ [M]: 239.07 Found: 239.1.

EXAMPLE 24. 3-C.HT .ORO-5-(4-(TRTFT ,I TOROMETHYT ,)PHF.NYT .)PYR AZTN-2- AMTNF, (3-24)

[0197] 5-(4-(trifluoromethyl)phenyl)pyrazin-2-amine 3-23 (1.637 g, 6.844 mmol) was stirred in dry DMF (15 mL) and N-chlorosuccinimide (1.005g, 7.53 mmol) was added. The reaction mixture was stirred at rt for 16 h and then extracted with sat. sodium thiosulfate and ethyl acetate. The organic layer was washed with water 3X, and then brine. The organic layer was concentrated under reduced pressure and the residue was purified via silica gel chromatography (ethyl acetate: hexanes) to afford 3-24 as a yellow solid (1.10 g, 59%). GCMS (El): Calc’d for C11H7CIF3N3 [M]: 273.6 Found: 273.0.

EXAMPLE 25. 3-CHLORO-N-(4-(TRIFLUOROMETHOXY)PHENYL)-5-(4-(TRIFLUOROMETHYL)PHENYL) PYR AZTN-2- AMTNF, (3-25)

[0198] A sealed vial was charged with Pd dba (9.2 mg, 5 mol percent), Xantphos (14 mg ,12 mol percent), l-iodo-4-(trifluoromethoxy)benzene (58 mg, 0.20 mmol), 3-24 (55 mg, 0.20 mmol) and CS2CO3 (82 mg 0.25 mmol). The flask was then evacuated and backfilled with argon 3X. Degassed anhydrous toluene (2 mL) was added through the septum. The mixture was stirred at 110 °C for 16 h and then allowed to cool to room temperature. After cooling, the solid material was filtered off and washed with ethyl acetate. The solvent was removed under reduced pressure and the residue was purified via silica gel chromatography (ethyl acetate: hexanes) to afford 3-25 as a clear yellow oil (82 mg, 92%). 'H NMR (400 MHz, Acetone-dg) d 8.78 (d, / = 0.3 Hz, 1H), 8.56 (s, 1H), 8.23 - 8.13 (m, 2H), 7.97 - 7.91 (m, 2H), 7.84 - 7.76 (m, 2H), 7.35 - 7.28 (m, 2H). ¹⁹F NMR (376 MHz, Acetone-dg) d -58.81 (s, 3F), - 63.07 (s, 3F).

EXAMPLE 26. 3-((4-(TRIFLUOROMETHOXY)PHENYL)AMINO)-6-(4-(TRIFLUOROMETHYL)PHENYL) PYRAZIN-2-OL (3-26)

[0199] 3-25 (60 mg, 0.14 mmol), KOH (78 mg, 1.4 mmol) were loaded in a sealed tube and dissolved with dioxane: water (1:1, 2 mL). The tube was sealed and stirred for 16 h at 140 °C. The reaction was allowed to cool to room temperature, acidified with HC1 (1M), extracted with ethyl acetate and washed with water. The organic layer was then dried with sodium sulfate, and solvent was removed under reduced pressure. The solid was then dissolved in minimal amounts of acetone, precipitated with hexanes, filtered and collected to afford 3-26 as a beige solid (14 mg, 24%). 'H NMR (400 MHz, Acetone-dg) d 11.17 (s, 1H), 8.86 (s, 1H), 8.26 - 8.18 (m, 2H), 8.05 - 7.89 (m, 2H), 7.88 - 7.77 (m, 2H), 7.43 (s, 1H), 7.38 - 7.26 (m, 2H). ¹⁹F NMR (376 MHz, Acetone-dg) d -58.87 (s, 3F), -63.15 (s, 3F). HRMS (ESI ): Calcd. for (CisHioFgNsCh-) [M-H] - : 414.2880 Found: 414.0683

EXAMPLE 27. BIOLOGIAL ACTIVITY OF COMPOUNDS

[0200] Biological activities of the compounds synthesized is determined by determining increase in oxygen consumption rate (OCR).

[0201] Oxygen consumption rate (OCR) in whole cells is measured in general accordance with the method of Kenwood BM et al. (Mol. Met. (2014) 3: 114-123).

[0202] OCR is measured using a Seahorse XF-24 Flux Analyzer (Seahorse Biosciences, North Billerica, MA). NMuLi, C2C12, and L6 cells are seeded in a Seahorse 24-well tissue culture plate at a density of 3.5xl0⁴ cells/well, isolated cardiomyocytes at a density of 4xl0⁴ cells/well, and human primary fibroblasts at a density of l.lxlO⁴ cells/well. The cells are then allowed to adhere for 24 h. Prior to the assay, the media is changed to unbuffered DMEM containing pyruvate and glutamine (Gibco #12800-017, pH=7.4 at 37 °C) and the cells are equilibrated for 30 mins at 37 °C. Compounds are injected during the assay and OCR is measured using 2 min measurement periods.

[0203] 2-3 wells are used per condition and averaged over three plates (n=6-9). Statistical significance is determined by two-way ANOVA with Bonferroni's posttest.

[0204] Compounds 3-18, 3-19, and 3-26 have observable activity in this assay.

EXAMPLE 24. DIET INDUCED OBESITY MOUSE STUDY

[0205] Male C57BL/6J mice aged 3 months (n = 6) are assigned to one of three treatment groups: normal chow diet (Chow), western diet (WD) or western diet containing compound 4c (WD+4c). Mice fed WD and WD+4c are individually housed and given 3 grams of fresh food daily. WD+4c contained a dose of 4c equivalent to 50 mg/kg/day. For all treatments pre -weighed food is placed in cages and food intake is calculated daily. Fat and lean mass are measured by EchoMRI.

[0206] Fat and lean mass for mice given the high fat Western Diet or the Western Diet with the mitochondrial uncoupler compound 4c was determined by EchoMRI. Mice receiving WD+4c gain less fat mass than WD control without losing lean mass and without a significant change in food intake. Certain compounds of the disclosure have anti-inflammatory effects in the STAM mouse model of fatty liver disease.

EXAMPLE 25.ROS PRODUCTION ASSAY

[0207] Certain compounds of the disclosure also decrease ROS production, which can be measured in this assay. L6 myoblasts are seeded into black-walled clear-bottom 96-well microplates in L6 growth media and grown to confluence. Cells are then washed twice with PBS and co-incubated with 7.5 mM CM-PEDCFDA and 0.5 ng/pL of each hit compound or vehicle control (DMSO) in KRP buffer (136 mM NaCl, 4.7 mM KC1, 10 mM NaP0₄, 0.9 mM MgS0₄, 0.9 mM CaCE, pH 7.4) supplemented with 25 mM D-glucose at 37° C. in 5% C0₂/95% air for 1 hr. 100 nM H2O2IS used as a positive control for ROS production. Following incubation, cells are washed three times with PBS to remove excess probe. Cells are then covered with 100 pL/well PBS and fluorescence intensity is measured by a Tecan Infinite®

M200 microplate reader (Tecan Group Ltd., Switzerland) using a top-read configuration and with the excitation and emission filters set at 495+9 nm and 530+20 nm, respectively. Fluorescence data are recorded on Magellan (version 6.4) software and exported to Microsoft Excel for subsequent analysis. After subtracting the background fluorescence (that emitted from a well which does not receive the CM- H2DCFDA probe) from each well, ROS production is expressed in terms of percentage fluorescence of the vehicle control for each condition. Compounds which increase ROS levels by greater than 20% are eliminated.

Claims

CLAIMS What is claimed is:

1. A compound of Formula I,

(Formula I)

or a pharmaceutically acceptable salt thereof, wherein:

X¹ and X² are chosen from N and CH, wherein at least one of X¹ and X² is N;

Z is absent (R² is bound to N) or Z is -C(=0)-;

R¹ is hydrogen or Ci-Csalkyl, C₂-Csalkenyl, or C₂-Csalkynyl;

R² is Ci-Csalkyl, C₂-Csalkenyl, or C₂-Csalkynyl; or

R² is -Co-C₄alkyl(C₃-C₇cycloalkyl), -Co-C₄alkyl(bridged C₇-Ci₂cycloalkyl),

-Co-C₄alkyl(aryl), -Co-C₄alkyl(mono- or bi-cyclic heteroaryl), or -Co-C₄alkyl(3- to 7- membered heterocycloalkyl), each of which is optionally substituted with one or more substituents independently chosen from R¹¹ and 0 or 1 substituents R¹²;

R³ is H or Ci-Csalkyl, C₂-Csalkenyl, or C₂-Csalkynyl, or

R³ is -Co-C₄alkyl(C₃-C₇cycloalkyl) or -Co-C₄alkyl(aryl), which is optionally substituted with one or more independently chosen R¹¹ substituents;

R⁴ and R⁵ are independently selected from halogen, hydroxyl, amino, nitro, cyano, -CHO, -COOH, Ci-C₂haloalkyl, Ci-C₂haloalkoxy, CVO.alkyl, CVO.alkoxy, C i-Cr, alkyl ester, -Co-C₄alkyl(mono- or di -C i -Cr,al kyl am i no) , C₂-C₆alkanoyl, C₂-C₆alkenyl, C₂-C₆alkynyl, aryl, optionally substituted with R¹³, and mono- or bicyclic heteroaryl, optionally substituted with R¹³;

wherein in each Co-C₄alkyl, Ci-Csalkyl, C Ci-Csalkyl, C₂-Csalkenyl, or C₂-Csalkynyl in the definitions of R¹, R², and R³ one or more carbon atoms is optionally replaced by O, NR¹⁰,

-C(O)-, -C(0)0-, -OC(O), -S(0)n-, -S(0)NR¹⁰-, -C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the Co-C₄alkyl, Ci-Cs alkyl, C₂-Csalkenyl, or C₂-Csalkynyl is optionally substituted with one or more substituents R¹³;

R¹⁰ is independently chosen at each occurrence from hydrogen, CVO, alkyl, and -Co-C₂alkyl(C₃- C₇cycloalkyl);

R¹¹ is independently selected at each occurrence from halogen, hydroxyl, amino, nitro, cyano, - CHO, -COOH, oxo, halosulfanyl, and Ci-Cioalkyl, C2-Csalkenyl, and C2-Csalkynyl, wherein in each Ci- Cioalkyl, C2-Csalkenyl, and C2-Csalkynyl, in the definition of Rⁿ one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-, -C(0)0-, -OC(O), -S(0)n-, -S(0)nNR¹⁰, -NR¹⁰S(O)n-, -NR¹⁰C(O)NR¹⁰, - C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which each Co-C4alkyl, Ci-Csalkyl, C2-Csalkenyl, or C2-Csalkynyl is optionally substituted with one or more substituents R¹³;

R¹² is selected from -Co-C4alkyl(C3-C7cycloalkyl), -0-Co-C₄alkyl(C₃-C₇cycloalkyl), -Co- C4alkyl(aryl), -0-Co-C₄alkyl(aryl), -Co-C₄alkyl(5- to 6-membered heteroaryl), -0-Co-C₄alkyl(5- to 6- membered heteroaryl), -Co-C₄alkyl(3- to 6-membered heterocycloalkyl), and -0-Co-C₄alkyl(3- to 6- membered heterocycloalkyl), each of which is optionally substituted with one or more substituents independently chosen from halogen, hydroxyl, amino, nitro, cyano, -CHO,

-COOH, oxo, Ci-C2haloalkyl, Ci-C2haloalkoxy, C i-Cr, alkyl, CVO.alkoxy, C i-Cr, alkyl ester, mono - or di- (Ci-C₆alkyl)carboxamide, -Co-C4alkyl(mono- or di -C i-Cr, alkyl ami no), C2-C6alkanoyl, C2-C6alkenyl, and CVCralkynyl; and

R¹³ is independently chosen at each occurrence from halogen, hydroxyl, amino, nitro, cyano, - CHO, -COOH, oxo, C3-C7cycloalkyl, and phenyl.

2. A compound or salt thereof of claim 1, wherein Z is absent and X¹ and X² are both nitrogen.

3. A compound or salt thereof of claim 1 , wherein Z is absent and one of X¹ and X² is nitrogen and the other is carbon.

4. A compound or salt thereof of any one of claims 1 to 3, wherein R¹ is hydrogen or unsubstituted C i-Cr, alkyl.

5. A compound or salt thereof of claim 4, wherein R¹ is hydrogen.

6. A compound or salt thereof of any one of claims 1 to 5, wherein R² is C i-C salkyl, C2- Csalkenyl, or C2-Csalkynyl; in each Co-C4alkyl, Ci-Csalkyl, C2-Csalkenyl, or C2-Csalkynyl one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-, -C(0)0-, -OC(O), -S(0)n-,

-C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the Co-C4alkyl, Ci-Cs alkyl, C2-Csalkenyl, or C2-Csalkynyl is optionally substituted with one or more substituents R¹³.

7. A compound or salt thereof of any one of claims 1 to 5, wherein R² is Cs-Cnalkyl, optionally substituted with one or more substituents independently chosen from halogen, hydroxyl, amino, nitro, cyano, and oxo.

8. A compound or salt thereof of any one of claims 1 to 5, wherein R²is -Co-C4alkyl(C3- C7cycloalkyl), -Co-C4alkyl(bridged C7-Ci2cycloalkyl), -Co-C4alkyl(aryl), -Co-C4alkyl(mono- or bi-cyclic heteroaryl), or -Co-C₄alkyl(4- to 7- membered heterocycloalkyl), each of which is optionally substituted with one or more substituents independently chosen from Rⁿ and 0 or 1 substituents R¹²;

in each Co-C4alkyl one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-,

-C(0)0-, -OC(O), -S(0)n-, -C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the C₀-C₄alkyl, Ci-Cs alkyl, C2-Csalkenyl, or C2-Csalkynyl is optionally substituted with one or more substituents R¹³.

9. A compound or salt thereof of claim 8, wherein

R² is -Co-C4alkyl(bridged C7-Ci2cycloalkyl) or -Co-C4alkyl(aryl), each of which is optionally substituted with one or more substituents independently chosen from R¹¹ and 0 or 1 substituents R¹²; in Co-C4alkyl one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-,

-C(0)0-, -OC(O), -S(0)n-, -C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the C₀-C₄alkyl is optionally substituted by R¹³.

10. A compound or salt thereof of claim 9, wherein

R² is phenyl, which is optionally substituted by one or more substituents independently chosen from R¹¹.

11. A compound or salt thereof of claim 9, wherein

R² is phenyl, which is substituted with one or more substituents independently chosen from halogen, hydroxyl, Ci-Cioalkyl, CVO.alkoxy, Ci-C2haloalkyl, and Ci-C2haloalkoxy.

12. A compound or salt thereof of claim 9 wherein:

R² is -Co-C4alkyl(phenyl), which is optionally substituted with one or more substituents independently chosen from R¹¹ and 1 substituent R¹²;

in Co-C4alkyl one or more carbon atoms is optionally replaced by O, NR¹⁰, -C(O)-,

-C(0)0-, -OC(O), -S(0)n-, -C(0)NR¹⁰-, or -NR¹⁰C(O)- where n is 0, 1, or 2, and in which the C₀-C₄alkyl is optionally substituted by R¹³; R¹² is selected from -Co-C4alkyl(C3-C7cycloalkyl), -0-Co-C₄alkyl(C₃-C₇cycloalkyl), -Co- C4alkyl(phenyl), -0-Co-C₄alkyl(phenyl), -Co-C₄alkyl(5- to 6-membered heteroaryl), -0-Co-C₄alkyl(5- to 6-membered heteroaryl), each of which is optionally substituted with one or more substituents independently chosen from halogen, hydroxyl, amino, nitro, cyano, -CHO,

-COOH, oxo, Ci-C2haloalkyl, Ci-C2haloalkoxy, C i-Cr, alkyl, CVO.alkoxy, C i-Cr, alkyl ester, -Co- C4alkyl(mono- or di-Ci-0,alkylamino), C2-C6alkanoyl, C2-C6alkenyl, and C2-C6alkynyl.

13. A compound or salt of claim 12, wherein

R² is phenyl, which is substituted with one substituent R¹²; and

R¹² is phenyl which is optionally substituted with one or more substituents independently chosen from halogen, hydroxyl, amino, nitro, cyano, -CHO, -COOH, oxo, Ci-C2haloalkyl, Ci-C2haloalkoxy, Ci- Csalkyl, CVO.alkoxy, CVO.alkylester, -Co-C4alkyl(mono- or di-C i-O, alkyl ami no), C2-C6alkanoyl, C2- Cealkenyl, and C2-C6alkynyl.

14. A compound or salt thereof of any one of claims 1 to 13, wherein

R³ is hydrogen.

15. A compound or salt thereof of any one of claims 1 to 13, wherein

R³ is Ci-Csalkyl, C2-Csalkenyl, or C2-Csalkynyl,

in Ci-Csalkyl, C2-Csalkenyl, or C2-Csalkynyl one or more carbon atoms is optionally replaced by O, NR¹⁰, C(0)0-, -OC(O), or -S(0)n-, where n is 0, 1, or 2, and in which the Ci-Cs alkyl, C2-Csalkenyl, or C2-Csalkynyl is optionally substituted with one or more substituents R¹³.

16. A compound or salt thereof of claim 15, wherein R³ is Ci-C_r, alkyl.

17. A compound or salt thereof of any one of claims 1 to 16, wherein

R⁴ and R⁵ are both hydrogen.

18. A compound or salt thereof of any one of claims 1 to 15, wherein

one of R⁴ and R⁵ is hydrogen, and the other is chosen from halogen, hydroxyl, Ci-C4alkyl, Ci- C4alkoxy, Ci-C2haloalkyl, and Ci-C2haloalkoxy.

19. A compound or salt thereof of claim 1, wherein

R¹ is hydrogen or Ci-C4alkyl; R² is C8-C12 alkyl; or

R² is phenyl, which is substituted with one or more substituents independently chosen from halogen, hydroxyl, Ci-Cioalkyl, CVO.alkoxy, Ci-C2haloalkyl, and Ci-C2haloalkoxy, or

R² is phenyl, which is substituted with one substituent R¹²; where R¹² is phenyl which is optionally substituted with one or more substituents independently chosen from halogen, hydroxyl, amino, nitro, cyano, -CHO, -COOH, oxo, Ci-C2haloalkyl, Ci-C2haloalkoxy, CVO.alkyl, CVO.alkoxy, Ci- C_r, alkyl ester, -Co-C4alkyl(mono- or di-CVO, alkyl ami no), C2-C6alkanoyl, C2-C6alkenyl, and CVOrilkynyl;

R³ is H or CVO.alkyl; and

R⁴ and R⁵ are both hydrogen or one of R⁴ and R⁵ is hydrogen, and the other is chosen from halogen, hydroxyl, Ci-C4alkyl, Ci-C4alkoxy, Ci-C2haloalkyl, and Ci-C2haloalkoxy.

20. A compound or salt thereof of claim 19 in which X¹ and X² are both N and Z is absent.

21. A compound or salt thereof of claim 1, wherein the compound is:

3 -(dodecylamino)pyrazin-2-ol ;

3-((4-decylphenyl)amino)pyrazin-2-ol;

3-((perfluorophenyl)amino)pyrazin-2-ol;

3-((2-fluorophenyl)amino)pyrazin-2-ol;

3-((4-(trifluoromethoxy)phenyl)amino)pyrazin-2-ol;

3 -((3 , 5 -bis(trifluoromethyl)phenyl) amino)pyr azin-2-ol ;

3-((4-(trifluoromethyl)phenyl)amino)pyrazin-2-ol;

3-((3-(trifluoromethyl)phenyl)amino)pyrazin-2-ol;

3-((3 '-methoxy- [1,1’-biphenyl] -3-yl)amino)pyrazin-2-ol;

3-((4'-fluoro-[l , r-biphenyl]-4-yl)amino)pyrazin-2-ol;

2-((4-(trifluoromethyl)phenyl)amino)pyridin-3-ol;

2-((3-(trifluoromethyl)phenyl)amino)pyridin-3-ol;

3-(benzyloxy)-/V-(4-(trifluoromethoxy)phenyl)-5-(trifluoromethyl)pyrazin-2-amine;

3 -((4-(trifluoromethoxy)phenyl) amino) -6 -(trifluoromethyl)pyr azin-2-ol ;

N-(5-bromo-3-hydroxypyrazin-2-yl)-3-fluorobenzamide;

N -(5 -bromo-3-hydroxypyrazin-2-yl)-2-fluorobenzamide ;

3-(benzyloxy)-/V-(4-(trifluoromethoxy)phenyl)-5-(trifluoromethyl)pyrazin-2-amine;

3 -((4-(trifluoromethoxy)phenyl) amino) -6 -(trifluoromethyl)pyr azin-2-ol ; or

3-((4-(trifluoromethoxy)phenyl)amino)-6-(4-(trifluoromethyl)phenyl) pyrazin-2-ol.

22. A pharmaceutical composition comprising a compound or salt thereof of any one of claims 1 to 21, together with a pharmaceutically acceptable carrier.

23. A method of treating or preventing a condition responsive to mitochondrial uncoupling, comprising administering a therapeutically effective amount of a compound or salt of any one of claims 1 to 21 to a patient in need of such treatment.

24. The method of claim 23, wherein the condition responsive to mitochondrial uncoupling is obesity, type II diabetes, fatty liver disease, insulin resistance, multiple sclerosis, cancer, Huntington’s disease, Alzheimer’s dementia, Parkinson’s disease, ischemia reperfusion injury, heart failure, non alcoholic fatty liver disease (NALFD), or non-alcoholic steatohepatitis (NASH)

25. A method of regulating glucose homeostasis or insulin action in a patient comprising administering a therapeutically effective amount of a compound or salt of any one of claim 1 to 21 to the patient.

26. A method of treating hyperlipidemia, glycemia, glucose tolerance, insulin sensitivity, adiposity, insulin resistance, obesity, or diabetes in a patient comprising administering a therapeutically effective amount of a compound of any one of claims 1 to 21 to the patient.

27. A method for decreasing the risk of cancer in a patient at risk for cancer, comprising administering a therapeutically effective amount of a compound of any one of claims 1 to 21 to the patient.

28. The method of claim 23, wherein the condition responsive to mitochondrial uncoupling is cancer and the cancer is a cancer having cancerous cells with impaired p53 expression or activity, a cancer with cancerous cells having a Ras mutation, a cancer with cancerous cells having a beta-catenin mutation, an adrenocortical carcinoma, melanoma, primary colon cancer, or a cancer with metastasis to the liver.